Register
Medicines reference
Active substance

Miconazole

Azole antifungal. Registered in Georgia: 4 veterinary products. Forms: ear drops.

Dose and use

Doses

We have no dose with a cited source for this substance yet.

Before use

Safety information

Known Contraindications

  • Critical
    Do not use if hypersensitive to miconazole or other azole antifungals.
    Sources: UK SPC
Latin name
Miconazole
Georgian name
მიკონაზოლი
Authorisation status
Authorised veterinary medicine
An authorised veterinary medicine containing this substance exists. Whether a particular use is on-label depends on the species and the indication - see each dose rule.
Registered in Georgia
4 of 4 forms
Human medicines in Georgia
Mikotran
Human medicines with this substance in the Georgian register of medicines (Ministry of Health), checked on 18 Oct 2026. They are human medicines, not veterinary products; strengths and forms differ.
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 18 Oct 2026
All forms and registration4

Registration in Georgia and abroad: the register, number, validity and source are behind (i).

Easotic, Ear drops

hydrocortisone aceponate 1.11 mg/ml + miconazole 15.1 mg/ml + gentamicin 1505 IU/ml, ear drops, suspension for dogs
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
7.8/10
Good
vetman assessment

Easotic

hydrocortisone aceponate 1.11 mg/ml + miconazole 15.1 mg/ml + gentamicin 1505 IU/ml, ear drops, suspension for dogs
Assessed clinical scopeDog · Labelled topical treatment of susceptible mixed bacterial and fungal otitis externa in dogs after otoscopy and ear cleaning · Into the ear
Care settingVeterinary-diagnosed outpatient otitis treatment
vetman score 7.8/10 Good
Evidence confidence: High Georgia: Yes, veterinary · Verified on 18 Oct 2026

A practical, evidence-supported short-course option for correctly diagnosed susceptible canine otitis externa; never use through a perforated tympanum.

Regulatory and scientific credibility8.5/10

The exact three-component ear suspension has a current September 2026 UK SPC and active Georgian veterinary registration, plus comparative clinical trial evidence.

Clinical efficacy8.0/10

The corticosteroid-antifungal-aminoglycoside combination addresses inflammation and susceptible mixed infection, with controlled trial support; cytology and response should determine antimicrobial fit.

Safety and tolerability6.5/10

An intact tympanum is mandatory because gentamicin is potentially ototoxic; hypersensitivity, generalised demodicosis and concurrent ototoxic treatment are hard restrictions.

Clinical practicality8.5/10

One calibrated pump per affected ear once daily for five days is simple and short, provided the canal is first cleaned, dried and examined.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Never use with a perforated tympanum; examine the ear before treatment.
  • Do not combine with other ototoxic substances or use in generalised demodicosis.
  • Use cytology and clinical response to confirm that a gentamicin-miconazole combination is justified.
Assessment sources
Assessed: 21 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Hydrocortisone aceponate1.11 mg/ml Miconazole15.1 mg/ml Gentamicin1505 IU/ml
Formulation Type
Ear drops
Administration route
Into the ear
Manufacturer
Virbac · France
Registration
Georgia Yes, veterinary
EU Yes, veterinary
№ EU/2/08/085
Verified on: 18 Oct 2026
UK Yes, veterinary
№ Vm 05653/5002
Verified on: 18 Oct 2026
US Yes, veterinary
№ NADA 141-330
Verified on: 18 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 18 Oct 2026

Otimix Plus, Ear drops

miconazole nitrate 23 mg/ml + polymyxin B sulfate 5500 IU/ml + prednisolone acetate 5 mg/ml, ear drops, suspension for dogs and cats
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in dogs, with primary dermatosis management
6.6/10
Situational / acceptable
vetman assessment

Otimix Plus

miconazole nitrate 23 mg/ml + polymyxin B sulfate 5500 IU/ml + prednisolone acetate 5 mg/ml, ear drops, suspension for dogs and cats
Assessed clinical scopeDog · Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in dogs, with primary dermatosis management · On the skin
Care settingVeterinary skin diagnosis with cytology/culture where indicated, clipping and limited-area twice-daily application with lick prevention and planned recheck
vetman score 6.6/10 Situational / acceptable
Evidence confidence: Low Georgia: Yes, veterinary · Verified on 22 Oct 2026

A plausible labelled option for culture-compatible limited infected dermatitis, but direct skin-outcome evidence is thin and steroid/AMEG-B exposure makes empirical or prolonged use unattractive.

Regulatory and scientific credibility8.0/10

The exact 15 ml dog/cat product has a current national EU regulator record, transparent exact instruction and Georgian registration; it is a generic of an established same-strength combination. Exact independent Otimix outcome/pharmacovigilance data and multi-country dossier breadth are limited.

Clinical efficacy6.0/10

The label and component spectrum support susceptible limited dermatitis, but direct modern canine outcomes for this fixed combination are sparse and broad empirical triple therapy is not justified. Primary allergic/parasitic disease and resistant organisms can defeat apparent short-term improvement.

Safety and tolerability6.0/10

Limited-area short-course exposure is usually manageable, but prednisolone can cause local immunosuppression, epidermal thinning, delayed healing and systemic adrenal effects with extensive, occluded, highly perfused or ingested use. Antimicrobial resistance and hypersensitivity remain.

Clinical practicality6.0/10

Ready-to-use drops and twice-daily limited-area application are workable, but clipping, gloves, full coverage, lick prevention and recheck are required; persistent fungal disease must transition away from steroid, making open-ended home continuation inappropriate.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Use only on a diagnosed limited susceptible dermatitis. Do not apply to an undiagnosed wound, extensive/ulcerated skin or under an impermeable dressing without a specific monitored plan.
  • Perform cytology and use culture/susceptibility when indicated. Polymyxin B is AMEG category B: reserve it for cases where category C/D antimicrobials are not expected to work; consider cross-resistance with colistin and other imidazoles.
  • Clip as needed, shake, cover the lesion with a few drops twice daily and rub with a gloved hand, generally no more than 14 days. Recheck cure and the underlying disease.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • For persistent fungal disease beyond the short labelled course, continue with a corticosteroid-free preparation if still indicated; do not prolong prednisolone merely because inflammation rebounds.
  • Otimix Plus is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone or excipients. Pregnancy/lactation safety is unestablished; use only after veterinarian benefit–risk assessment.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Store below 25°C and discard three months after first opening. Document opening date, course, organism/susceptibility basis and recheck result; do not keep using a contaminated communal bottle.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Dog Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in dogs, with intact tympanum and cause-directed management
6.9/10
Situational / acceptable
vetman assessment

Otimix Plus

miconazole nitrate 23 mg/ml + polymyxin B sulfate 5500 IU/ml + prednisolone acetate 5 mg/ml, ear drops, suspension for dogs and cats
Assessed clinical scopeDog · Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in dogs, with intact tympanum and cause-directed management · Into the ear
Care settingVeterinary otoscopy/cytology, intact tympanum confirmation, cleaning and susceptibility-led selection; instructed twice-daily application with massage and planned clinical/cytological recheck
vetman score 6.9/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · Verified on 22 Oct 2026

An evidence-supported but stewardship-restricted triple ear drop for susceptible external otitis with an intact tympanum. It is useful when diagnostics fit, not a default for every inflamed ear.

Regulatory and scientific credibility8.0/10

The exact 15 ml dog/cat product has a current national EU regulator record, transparent exact instruction and Georgian registration; it is a generic of an established same-strength combination. Exact independent Otimix outcome/pharmacovigilance data and multi-country dossier breadth are limited.

Clinical efficacy7.5/10

Multiple controlled trials of the same three-active combination support canine otitis efficacy, but cure is not universal and modern trials show suitable alternatives can match or outperform it. Activity depends on actual susceptibility, cleaning and correction of primary disease.

Safety and tolerability5.5/10

An intact tympanum is a hard prerequisite because polymyxin B is potentially ototoxic; very rare deafness is reported and steroid/antimicrobial exposure can mask or select persistent infection. Local/systemic corticosteroid effects, hypersensitivity and pregnancy uncertainty remain.

Clinical practicality6.5/10

Three to five drops twice daily for 7–14 days is familiar and feasible after cleaning, but requires reliable home adherence, massage, dropper hygiene and recheck. Otoscopy/intact-tympanum confirmation and AMEG-B susceptibility justification add necessary clinical work.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Never use unless otoscopy confirms an intact tympanum. Polymyxin B is potentially ototoxic; perforation, suspected middle-ear disease, new vestibular signs or hearing change requires stopping and immediate reassessment.
  • Perform cytology and use culture/susceptibility when indicated. Polymyxin B is AMEG category B: reserve it for cases where category C/D antimicrobials are not expected to work; consider cross-resistance with colistin and other imidazoles.
  • Clean the external canal, shake well, apply 3–5 drops twice daily and massage the base. Treat at least 7–10 and no more than 14 days, with clinical and cytological recheck rather than stopping on appearance alone.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • Very rare deafness is reported, especially in older dogs. Stop for new hearing loss, head tilt, nystagmus, ataxia or severe pain and investigate otitis media/interna.
  • Otimix Plus is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone or excipients. Pregnancy/lactation safety is unestablished; use only after veterinarian benefit–risk assessment.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Store below 25°C and discard three months after first opening. Document opening date, course, organism/susceptibility basis and recheck result; do not keep using a contaminated communal bottle.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in cats, with primary dermatosis management
6.2/10
Situational / acceptable
vetman assessment

Otimix Plus

miconazole nitrate 23 mg/ml + polymyxin B sulfate 5500 IU/ml + prednisolone acetate 5 mg/ml, ear drops, suspension for dogs and cats
Assessed clinical scopeCat · Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in cats, with primary dermatosis management · On the skin
Care settingVeterinary skin diagnosis with cytology/culture where indicated, clipping and limited-area twice-daily application with lick prevention and planned recheck
vetman score 6.2/10 Situational / acceptable
Evidence confidence: Low Georgia: Yes, veterinary · Verified on 22 Oct 2026

A weakly evidenced feline skin option whose fixed antibiotic-antifungal-steroid mix, grooming exposure and imprecise lesion dose justify narrow, reassessed use only.

Regulatory and scientific credibility8.0/10

The exact 15 ml dog/cat product has a current national EU regulator record, transparent exact instruction and Georgian registration; it is a generic of an established same-strength combination. Exact independent Otimix outcome/pharmacovigilance data and multi-country dossier breadth are limited.

Clinical efficacy5.5/10

The feline dermatitis indication is regulator-supported, but direct outcome evidence is very limited and grooming increases exposure. Cytology/culture and diagnosis of the primary dermatosis are essential; short-term steroid improvement does not prove infection cure.

Safety and tolerability5.5/10

Skin exposure plus grooming/ingestion increases local and systemic corticosteroid uncertainty in cats. Immunosuppression, delayed healing, secondary infection, resistance and hypersensitivity require a limited area, short course and lick prevention.

Clinical practicality5.5/10

Twice-daily lesion coverage, clipping and lick prevention are difficult in many cats, while an imprecise “few drops” skin dose complicates consistent exposure. Gloves, recheck and switching away from steroid for persistent fungal disease add burden.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Use only on a diagnosed limited susceptible dermatitis. Do not apply to an undiagnosed wound, extensive/ulcerated skin or under an impermeable dressing without a specific monitored plan.
  • Perform cytology and use culture/susceptibility when indicated. Polymyxin B is AMEG category B: reserve it for cases where category C/D antimicrobials are not expected to work; consider cross-resistance with colistin and other imidazoles.
  • Clip as needed, shake, cover the lesion with a few drops twice daily and rub with a gloved hand, generally no more than 14 days. Recheck cure and the underlying disease.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • For persistent fungal disease beyond the short labelled course, continue with a corticosteroid-free preparation if still indicated; do not prolong prednisolone merely because inflammation rebounds.
  • Otimix Plus is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone or excipients. Pregnancy/lactation safety is unestablished; use only after veterinarian benefit–risk assessment.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Store below 25°C and discard three months after first opening. Document opening date, course, organism/susceptibility basis and recheck result; do not keep using a contaminated communal bottle.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in cats, with intact tympanum and cause-directed management
6.6/10
Situational / acceptable
vetman assessment

Otimix Plus

miconazole nitrate 23 mg/ml + polymyxin B sulfate 5500 IU/ml + prednisolone acetate 5 mg/ml, ear drops, suspension for dogs and cats
Assessed clinical scopeCat · Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in cats, with intact tympanum and cause-directed management · Into the ear
Care settingVeterinary otoscopy/cytology, intact tympanum confirmation, cleaning and susceptibility-led selection; instructed twice-daily application with massage and planned clinical/cytological recheck
vetman score 6.6/10 Situational / acceptable
Evidence confidence: Low Georgia: Yes, veterinary · Verified on 22 Oct 2026

A regulator-supported feline option, but independent feline outcomes are limited and repeated handling plus ototoxicity/stewardship constraints make it conditional.

Regulatory and scientific credibility8.0/10

The exact 15 ml dog/cat product has a current national EU regulator record, transparent exact instruction and Georgian registration; it is a generic of an established same-strength combination. Exact independent Otimix outcome/pharmacovigilance data and multi-country dossier breadth are limited.

Clinical efficacy6.5/10

The exact label includes cats and mixed-species Otodectes plus limited feline reports support the same combination, but independent feline bacterial/fungal otitis outcomes are sparse. The product is only adjunctive for ear mites and susceptibility/primary disease remain decisive.

Safety and tolerability5.5/10

An intact tympanum is a hard prerequisite because polymyxin B is potentially ototoxic; very rare deafness is reported and steroid/antimicrobial exposure can mask or select persistent infection. Local/systemic corticosteroid effects, hypersensitivity and pregnancy uncertainty remain.

Clinical practicality6.0/10

The same small-volume twice-daily regimen is feasible, but many cats resist ear handling for 7–14 days. Safe restraint, cleaning, massage, dropper hygiene, cytological recheck and intact-tympanum confirmation create a meaningful adherence and welfare burden.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Never use unless otoscopy confirms an intact tympanum. Polymyxin B is potentially ototoxic; perforation, suspected middle-ear disease, new vestibular signs or hearing change requires stopping and immediate reassessment.
  • Perform cytology and use culture/susceptibility when indicated. Polymyxin B is AMEG category B: reserve it for cases where category C/D antimicrobials are not expected to work; consider cross-resistance with colistin and other imidazoles.
  • Clean the external canal, shake well, apply 3–5 drops twice daily and massage the base. Treat at least 7–10 and no more than 14 days, with clinical and cytological recheck rather than stopping on appearance alone.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • Very rare deafness is reported, especially in older dogs. Stop for new hearing loss, head tilt, nystagmus, ataxia or severe pain and investigate otitis media/interna.
  • Otimix Plus is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone or excipients. Pregnancy/lactation safety is unestablished; use only after veterinarian benefit–risk assessment.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Store below 25°C and discard three months after first opening. Document opening date, course, organism/susceptibility basis and recheck result; do not keep using a contaminated communal bottle.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Miconazole23 mg/ml Polymyxin B5500 IU/ml Prednisolone5 mg/ml
Formulation Type
Ear drops
Administration route
Into the ear, On the skin
Manufacturer
Bioveta a.s. · Czechia
Registration
Georgia Yes, veterinary
EU Yes, veterinary
№ CZ 96/053/23-C
Verified on: 22 Oct 2026
UK No
US No
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 18 Oct 2026
Information not fully verified Shake well. Otitis: after cytology/otoscopy, cleaning and confirmation of intact tympanum, apply 3–5 drops into the affected external canal twice daily and massage; continue a few days after signs resolve, at least 7–10 and at most 14 days. Dermatitis: clip as needed, cover the lesion with a few drops twice daily and rub with a gloved hand, usually no more than 14 days; persistent fungal treatment should continue without corticosteroid. Recheck clinical and cytological cure.

OTOPET THERAPY, Ear drops

rifaximin 10 mg/ml + colistin sulfate 200000 IU/ml + miconazole 17.4 mg/ml + carbaryl 10 mg/ml + triamcinolone 0.908 mg/ml, ear drops for dogs and cats
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog Complete authorised canine scope: external otitis associated with susceptible bacteria, fungi/yeasts, ear mites or inflammation
6.1/10
Situational / acceptable
vetman assessment

OTOPET THERAPY

rifaximin 10 mg/ml + colistin sulfate 200000 IU/ml + miconazole 17.4 mg/ml + carbaryl 10 mg/ml + triamcinolone 0.908 mg/ml, ear drops for dogs and cats
Assessed clinical scopeDog · Complete authorised canine scope: external otitis associated with susceptible bacteria, fungi/yeasts, ear mites or inflammation · Into the ear
Care settingVeterinary otoscopy/cytology-led treatment with careful cleaning, intact-tympanum confirmation, owner twice-daily application and clinical/cytologic recheck
vetman score 6.1/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · № 1-03/44 · Verified on 23 Oct 2026

A situational five-active canine otic option when otoscopy and cytology genuinely support its relevant antibacterial, antifungal, acaricidal and steroid components. It should not be a default for every inflamed ear; no direct modern exact-product outcome programme was found, and tympanic, carbaryl, steroid and stewardship risks require controls.

Regulatory and scientific credibility8.5/10

Exact rifaximin 10 mg/ml, colistin sulfate 200,000 IU/ml, miconazole 17.4 mg/ml, carbaryl 10 mg/ml and triamcinolone 0.908 mg/ml identity, dog/cat route, regimen and perforation/handler restrictions are transparent in current Georgian and multiple current EU regulator records. Credibility is reduced by legacy development, no public modern exact-product assessment or quantified adverse-event/outcome dossier, and a broad inflammation-only label scope that conflicts with current stewardship.

Clinical efficacy6.0/10

Antibacterial, antifungal, acaricidal and anti-inflammatory components are mechanistically plausible for mixed canine otitis, and topical combination therapy is established when cytology supports it. No controlled exact-product outcome study was found, each component is not needed in every ear, and inflammation-only, resistant-rod, primary allergic or middle-ear disease is not solved by blanket five-active exposure.

Safety and tolerability4.5/10

The label reports no adverse reactions and permits reproduction, but modern quantified exact safety evidence is absent. Perforation is contraindicated; colistin/polymyxin-class ototoxicity concern, carbaryl cholinesterase inhibition/dermal absorption, topical steroid effects, contact irritation and dual-antibiotic selection pressure require active controls.

Clinical practicality5.0/10

A fixed 1-2 ml per ear avoids weight calculation and massage aids distribution. Twice-daily shaking, careful cleaning, relatively large oily volume for 7-10 days, restraint/handling, gloves, tympanum examination, cytology and recheck are substantial burdens; canal size makes the twofold volume range a clinician decision rather than a simple owner rule.

Full-course cost-effectiveness-

Current Georgian course price was unavailable; price is excluded from the denominator.

Important safety and use flags

  • Scope boundary: this canine score covers the full labelled external-otitis scope. It does not cover otitis media/interna, every inflamed ear, undiagnosed neurologic signs or use in another species.
  • Examine before treating: perform otoscopy, confirm an intact tympanic membrane and obtain cytology in every case (stained dry mount plus mite wet mount as appropriate). Culture/susceptibility is important with rods, chronic/recurrent disease, prior antimicrobial exposure or poor response.
  • Cause-directed care: identify allergy, foreign body, conformation, keratinisation/endocrine disease, polyp/mass, parasites or middle-ear disease. Antimicrobials treat secondary overgrowth/infection but do not correct the primary driver of recurrence.
  • Exact administration: shake well, clean carefully, instil 1-2 ml into each affected external canal and massage twice daily for 7-10 days. This is a clinician-selected fixed per-ear range, not a body-weight calculator; do not place it in an unexamined/perforated ear.
  • Stewardship: do not expose a cytology-negative merely inflamed ear to rifaximin, colistin and miconazole by default. At recheck, narrow/stop/switch according to clinical and cytologic response; persistent rods require culture and a documented plan rather than repeated empirical courses.
  • Parasitic boundary: repeat the course after 10 days only for confirmed/suspected parasitic otitis under the label plan. Confirm Otodectes, examine/treat relevant in-contact animals and manage the environment; this repeat instruction is not for every bacterial or yeast episode.
  • Tympanic/neurologic safety: stop and urgently reassess hearing loss, head tilt, nystagmus, ataxia, facial/Horner signs, severe pain or neurologic deterioration. Perforation is contraindicated and suspected middle-ear disease needs sampling/imaging/appropriate non-ototoxic care.
  • Carbaryl safety: wear impermeable gloves and avoid skin/eye contact. Review organophosphates and other cholinesterase inhibitors; hypersalivation, vomiting/diarrhoea, miosis, fasciculation, weakness, dyspnoea or seizure may indicate systemic cholinergic toxicity.
  • Dog safety/recheck: stop for marked irritation, worsening erythema/exudate, systemic steroid effects or hypersensitivity. Recheck clinical signs and cytology; visible improvement alone does not prove microbial resolution or control of allergic disease.
  • Reproduction and handling boundary: the exact label permits pregnancy and lactation at the recommended regimen, but modern quantified exact-product safety data are limited. Prevent licking/eye exposure, wash hands after use, keep the bottle from children and dispose as veterinary waste.
Assessment sources
Assessed: 23 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Complete authorised feline scope: external otitis associated with susceptible bacteria, fungi/yeasts, ear mites or inflammation
5.7/10
Weak evidence support
vetman assessment

OTOPET THERAPY

rifaximin 10 mg/ml + colistin sulfate 200000 IU/ml + miconazole 17.4 mg/ml + carbaryl 10 mg/ml + triamcinolone 0.908 mg/ml, ear drops for dogs and cats
Assessed clinical scopeCat · Complete authorised feline scope: external otitis associated with susceptible bacteria, fungi/yeasts, ear mites or inflammation · Into the ear
Care settingVeterinary otoscopy/cytology-led treatment with careful cleaning, intact-tympanum confirmation, owner twice-daily application and clinical/cytologic recheck
vetman score 5.7/10 Weak evidence support
Evidence confidence: Medium Georgia: Yes, veterinary · № 1-03/44 · Verified on 23 Oct 2026

A weak, highly selective feline otic option when mites and/or matching secondary microbes are documented and the tympanic membrane is intact. The absence of direct feline exact-product outcomes, broad inflammation-only label, contact-reaction concern and complex five-active safety/stewardship burden keep the score low.

Regulatory and scientific credibility8.5/10

Exact rifaximin 10 mg/ml, colistin sulfate 200,000 IU/ml, miconazole 17.4 mg/ml, carbaryl 10 mg/ml and triamcinolone 0.908 mg/ml identity, dog/cat route, regimen and perforation/handler restrictions are transparent in current Georgian and multiple current EU regulator records. Credibility is reduced by legacy development, no public modern exact-product assessment or quantified adverse-event/outcome dossier, and a broad inflammation-only label scope that conflicts with current stewardship.

Clinical efficacy5.0/10

The component roles are plausible, especially for confirmed Otodectes with secondary microbial inflammation, but no controlled exact-product feline outcome study was found. Feline otitis more often requires targeted investigation for mites, polyps, masses or middle-ear disease, and a broad five-active mixture for cytology-negative inflammation has a particularly weak evidence basis.

Safety and tolerability4.0/10

The label reports no adverse reactions and permits reproduction, but modern quantified feline safety evidence is absent. Cats may be particularly prone to otic contact reactions; perforation/ototoxicity, carbaryl systemic cholinergic exposure, topical steroid effects and unnecessary dual-antibiotic exposure make the safety ceiling lower than in dogs.

Clinical practicality5.0/10

A fixed 1-2 ml per ear avoids weight calculation and massage aids distribution. Twice-daily shaking, careful cleaning, relatively large oily volume for 7-10 days, restraint/handling, gloves, tympanum examination, cytology and recheck are substantial burdens; canal size makes the twofold volume range a clinician decision rather than a simple owner rule.

Full-course cost-effectiveness-

Current Georgian course price was unavailable; price is excluded from the denominator.

Important safety and use flags

  • Scope boundary: this feline score covers the full labelled external-otitis scope. It does not cover otitis media/interna, every inflamed ear, undiagnosed neurologic signs or use in another species.
  • Examine before treating: perform otoscopy, confirm an intact tympanic membrane and obtain cytology in every case (stained dry mount plus mite wet mount as appropriate). Culture/susceptibility is important with rods, chronic/recurrent disease, prior antimicrobial exposure or poor response.
  • Cause-directed care: identify allergy, foreign body, conformation, keratinisation/endocrine disease, polyp/mass, parasites or middle-ear disease. Antimicrobials treat secondary overgrowth/infection but do not correct the primary driver of recurrence.
  • Exact administration: shake well, clean carefully, instil 1-2 ml into each affected external canal and massage twice daily for 7-10 days. This is a clinician-selected fixed per-ear range, not a body-weight calculator; do not place it in an unexamined/perforated ear.
  • Stewardship: do not expose a cytology-negative merely inflamed ear to rifaximin, colistin and miconazole by default. At recheck, narrow/stop/switch according to clinical and cytologic response; persistent rods require culture and a documented plan rather than repeated empirical courses.
  • Parasitic boundary: repeat the course after 10 days only for confirmed/suspected parasitic otitis under the label plan. Confirm Otodectes, examine/treat relevant in-contact animals and manage the environment; this repeat instruction is not for every bacterial or yeast episode.
  • Tympanic/neurologic safety: stop and urgently reassess hearing loss, head tilt, nystagmus, ataxia, facial/Horner signs, severe pain or neurologic deterioration. Perforation is contraindicated and suspected middle-ear disease needs sampling/imaging/appropriate non-ototoxic care.
  • Carbaryl safety: wear impermeable gloves and avoid skin/eye contact. Review organophosphates and other cholinesterase inhibitors; hypersalivation, vomiting/diarrhoea, miosis, fasciculation, weakness, dyspnoea or seizure may indicate systemic cholinergic toxicity.
  • Feline contact-reaction warning: cats may deteriorate from topical contact dermatitis. Stop if erythema, suppuration, pruritus or pain worsens despite improving cytology; investigate polyp/mass and middle-ear disease rather than layering additional products.
  • Reproduction and handling boundary: the exact label permits pregnancy and lactation at the recommended regimen, but modern quantified exact-product safety data are limited. Prevent licking/eye exposure, wash hands after use, keep the bottle from children and dispose as veterinary waste.
Assessment sources
Assessed: 23 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Rifaximin10 mg/ml Colistin200000 IU/ml Miconazole17.4 mg/ml Carbaryl10 mg/ml Triamcinolone0.908 mg/ml
Formulation Type
Ear drops
Administration route
Into the ear
Manufacturer
Fatro S.p.A. · Italy
Manufacturer (register)
FATRO S.p.A. Ltd, Italy
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 36, 19 Oct 2026.
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ოტოპეტ თერაპი
№ 1-03/44
Verified on: 23 Oct 2026
EU Yes, veterinary
№ V/NRP/02/1490; 96/019/00-C; 96/151/99-S
Verified on: 23 Oct 2026
UK No
US No
Controlled in Georgia
Unknown
Information not fully verified Complete labelled scope: dog/cat otitis externa associated with susceptible bacteria, fungi/yeasts, ear mites or inflammation. Shake, clean carefully, instil 1-2 ml per affected external canal and massage twice daily for 7-10 days; repeat after 10 days only for parasitic otitis. This is a fixed per-ear volume, not a body-weight dose. Cytology and otoscopy determine whether the five-active combination is appropriate; recheck to documented resolution.

Ototop, Ear drops

miconazole nitrate 23 mg/ml + prednisolone acetate 5 mg/ml + polymyxin B sulfate 5500 IU/ml, ear drops and cutaneous suspension
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in dogs, with primary dermatosis management
6.7/10
Situational / acceptable
vetman assessment

Ototop

miconazole nitrate 23 mg/ml + prednisolone acetate 5 mg/ml + polymyxin B sulfate 5500 IU/ml, ear drops and cutaneous suspension
Assessed clinical scopeDog · Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in dogs, with primary dermatosis management · On the skin
Care settingVeterinary skin diagnosis with cytology/culture where indicated, clipping and limited-area twice-daily application with lick prevention and planned recheck
vetman score 6.7/10 Situational / acceptable
Evidence confidence: Medium Georgia: Yes, veterinary · Verified on 22 Oct 2026

A plausible labelled option for culture-compatible limited infected dermatitis, but direct skin-outcome evidence is thin and steroid/AMEG-B exposure makes empirical or prolonged use unattractive.

Regulatory and scientific credibility8.5/10

The exact dog/cat product has a current regulator leaflet, valid multi-country EU DCP, transparent three-pack identity, national-register corroboration and Georgian registration. The established same-strength combination has independent controls, although direct independent Ototop outcome data remain limited.

Clinical efficacy6.0/10

The label and component spectrum support susceptible limited dermatitis, but direct modern canine outcomes for this fixed combination are sparse and broad empirical triple therapy is not justified. Primary allergic/parasitic disease and resistant organisms can defeat apparent short-term improvement.

Safety and tolerability6.0/10

Limited-area short-course exposure is usually manageable, but prednisolone can cause local immunosuppression, epidermal thinning, delayed healing and systemic adrenal effects with extensive, occluded, highly perfused or ingested use. Antimicrobial resistance and hypersensitivity remain.

Clinical practicality6.0/10

Ready-to-use suspension and twice-daily thin-film application are workable, but clipping, gloves, full coverage, lick prevention and recheck are required; persistent fungal disease must transition away from steroid, making open-ended home continuation inappropriate.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Use only on a diagnosed limited susceptible dermatitis. The exact label prohibits extensive lesions, poorly healing or fresh wounds and viral skin infections; avoid occlusion or an undiagnosed lesion.
  • Perform organism identification and susceptibility testing when possible. Polymyxin B is AMEG category B: prefer an effective lower-category option; known polymyxin B or miconazole resistance excludes use.
  • Clip and clean as needed, shake, apply a thin film twice daily and rub in, normally no more than 14 days. Persistent signs may require 2–3 weeks only with repeated examination and diagnostic verification; no numeric skin drop count is stated.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • For persistent fungal disease beyond the short labelled course, continue with a corticosteroid-free preparation if still indicated; do not prolong prednisolone merely because inflammation rebounds.
  • Ototop is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone, related corticosteroids/azoles or excipients. Pregnancy/lactation safety is unestablished; use only after veterinary benefit–risk assessment and avoid mammary-gland application.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Do not mix with another veterinary medicine because compatibility studies are absent. Store below 25°C and discard six months after first opening; document opening date, course, susceptibility basis and recheck result.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Dog Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in dogs, with intact tympanum and cause-directed management
7.1/10
Good
vetman assessment

Ototop

miconazole nitrate 23 mg/ml + prednisolone acetate 5 mg/ml + polymyxin B sulfate 5500 IU/ml, ear drops and cutaneous suspension
Assessed clinical scopeDog · Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in dogs, with intact tympanum and cause-directed management · Into the ear
Care settingVeterinary otoscopy/cytology, intact tympanum confirmation, cleaning and susceptibility-led selection; instructed twice-daily application with massage and planned clinical/cytological recheck
vetman score 7.1/10 Good
Evidence confidence: Medium Georgia: Yes, veterinary · Verified on 22 Oct 2026

An evidence-supported but stewardship-restricted triple ear drop for susceptible external otitis with an intact tympanum. It is useful when diagnostics fit, not a default for every inflamed ear.

Regulatory and scientific credibility8.5/10

The exact dog/cat product has a current regulator leaflet, valid multi-country EU DCP, transparent three-pack identity, national-register corroboration and Georgian registration. The established same-strength combination has independent controls, although direct independent Ototop outcome data remain limited.

Clinical efficacy7.5/10

Multiple controlled trials of the same three-active combination support canine otitis efficacy, but cure is not universal and modern trials show suitable alternatives can match or outperform it. Activity depends on actual susceptibility, cleaning and correction of primary disease.

Safety and tolerability5.5/10

An intact tympanum is a hard prerequisite because polymyxin B is potentially ototoxic; very rare deafness is reported and steroid/antimicrobial exposure can mask or select persistent infection. Local/systemic corticosteroid effects, hypersensitivity and pregnancy uncertainty remain.

Clinical practicality6.5/10

Three to five drops twice daily for 7–14 days is familiar and feasible after cleaning, but requires reliable home adherence, massage, dropper hygiene and recheck. Otoscopy/intact-tympanum confirmation and AMEG-B susceptibility justification add necessary clinical work.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Never use unless otoscopy confirms an intact tympanum. Polymyxin B is potentially ototoxic; perforation, suspected middle-ear disease, new vestibular signs or hearing change requires stopping and immediate reassessment.
  • Perform organism identification and susceptibility testing when possible. Polymyxin B is AMEG category B: prefer an effective lower-category option; known polymyxin B or miconazole resistance excludes use.
  • Clean the external canal, shake well, apply 3–5 drops (0.035 ml/drop) twice daily and massage. Continue uninterrupted for several days after complete clinical resolution, at least 7 and at most 14 days; veterinary confirmation of cure is required before stopping.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • Very rare deafness is reported, especially in older dogs. Stop for new hearing loss, head tilt, nystagmus, ataxia or severe pain and investigate otitis media/interna.
  • Ototop is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone, related corticosteroids/azoles or excipients. Pregnancy/lactation safety is unestablished; use only after veterinary benefit–risk assessment and avoid mammary-gland application.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Do not mix with another veterinary medicine because compatibility studies are absent. Store below 25°C and discard six months after first opening; document opening date, course, susceptibility basis and recheck result.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in cats, with primary dermatosis management
6.3/10
Situational / acceptable
vetman assessment

Ototop

miconazole nitrate 23 mg/ml + prednisolone acetate 5 mg/ml + polymyxin B sulfate 5500 IU/ml, ear drops and cutaneous suspension
Assessed clinical scopeCat · Label-concordant topical treatment of limited dermatitis caused by susceptible bacterial/fungal organisms in cats, with primary dermatosis management · On the skin
Care settingVeterinary skin diagnosis with cytology/culture where indicated, clipping and limited-area twice-daily application with lick prevention and planned recheck
vetman score 6.3/10 Situational / acceptable
Evidence confidence: Low Georgia: Yes, veterinary · Verified on 22 Oct 2026

A weakly evidenced feline skin option whose fixed antibiotic-antifungal-steroid mix, grooming exposure and imprecise lesion dose justify narrow, reassessed use only.

Regulatory and scientific credibility8.5/10

The exact dog/cat product has a current regulator leaflet, valid multi-country EU DCP, transparent three-pack identity, national-register corroboration and Georgian registration. The established same-strength combination has independent controls, although direct independent Ototop outcome data remain limited.

Clinical efficacy5.5/10

The feline dermatitis indication is regulator-supported, but direct outcome evidence is very limited and grooming increases exposure. Cytology/culture and diagnosis of the primary dermatosis are essential; short-term steroid improvement does not prove infection cure.

Safety and tolerability5.5/10

Skin exposure plus grooming/ingestion increases local and systemic corticosteroid uncertainty in cats. Immunosuppression, delayed healing, secondary infection, resistance and hypersensitivity require a limited area, short course and lick prevention.

Clinical practicality5.5/10

Twice-daily thin-film coverage, clipping and lick prevention are difficult in many cats, while the absence of a numeric skin volume requires careful lesion-based application. Gloves, recheck and switching away from steroid for persistent fungal disease add burden.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Use only on a diagnosed limited susceptible dermatitis. The exact label prohibits extensive lesions, poorly healing or fresh wounds and viral skin infections; avoid occlusion or an undiagnosed lesion.
  • Perform organism identification and susceptibility testing when possible. Polymyxin B is AMEG category B: prefer an effective lower-category option; known polymyxin B or miconazole resistance excludes use.
  • Clip and clean as needed, shake, apply a thin film twice daily and rub in, normally no more than 14 days. Persistent signs may require 2–3 weeks only with repeated examination and diagnostic verification; no numeric skin drop count is stated.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • For persistent fungal disease beyond the short labelled course, continue with a corticosteroid-free preparation if still indicated; do not prolong prednisolone merely because inflammation rebounds.
  • Ototop is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone, related corticosteroids/azoles or excipients. Pregnancy/lactation safety is unestablished; use only after veterinary benefit–risk assessment and avoid mammary-gland application.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Do not mix with another veterinary medicine because compatibility studies are absent. Store below 25°C and discard six months after first opening; document opening date, course, susceptibility basis and recheck result.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Cat Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in cats, with intact tympanum and cause-directed management
6.7/10
Situational / acceptable
vetman assessment

Ototop

miconazole nitrate 23 mg/ml + prednisolone acetate 5 mg/ml + polymyxin B sulfate 5500 IU/ml, ear drops and cutaneous suspension
Assessed clinical scopeCat · Label-concordant treatment of external otitis caused by susceptible bacterial/fungal organisms in cats, with intact tympanum and cause-directed management · Into the ear
Care settingVeterinary otoscopy/cytology, intact tympanum confirmation, cleaning and susceptibility-led selection; instructed twice-daily application with massage and planned clinical/cytological recheck
vetman score 6.7/10 Situational / acceptable
Evidence confidence: Low Georgia: Yes, veterinary · Verified on 22 Oct 2026

A regulator-supported feline option, but independent feline outcomes are limited and repeated handling plus ototoxicity/stewardship constraints make it conditional.

Regulatory and scientific credibility8.5/10

The exact dog/cat product has a current regulator leaflet, valid multi-country EU DCP, transparent three-pack identity, national-register corroboration and Georgian registration. The established same-strength combination has independent controls, although direct independent Ototop outcome data remain limited.

Clinical efficacy6.5/10

The exact label includes cats and mixed-species Otodectes plus limited feline reports support the same combination, but independent feline bacterial/fungal otitis outcomes are sparse. The product is only adjunctive for ear mites and susceptibility/primary disease remain decisive.

Safety and tolerability5.5/10

An intact tympanum is a hard prerequisite because polymyxin B is potentially ototoxic; very rare deafness is reported and steroid/antimicrobial exposure can mask or select persistent infection. Local/systemic corticosteroid effects, hypersensitivity and pregnancy uncertainty remain.

Clinical practicality6.0/10

The same small-volume twice-daily regimen is feasible, but many cats resist ear handling for 7–14 days. Safe restraint, cleaning, massage, dropper hygiene, clinical recheck and intact-tympanum confirmation create a meaningful adherence and welfare burden.

Full-course cost-effectiveness-

Current Georgian full-course price and pack-wastage data were unavailable; price is excluded from the denominator.

Important safety and use flags

  • Never use unless otoscopy confirms an intact tympanum. Polymyxin B is potentially ototoxic; perforation, suspected middle-ear disease, new vestibular signs or hearing change requires stopping and immediate reassessment.
  • Perform organism identification and susceptibility testing when possible. Polymyxin B is AMEG category B: prefer an effective lower-category option; known polymyxin B or miconazole resistance excludes use.
  • Clean the external canal, shake well, apply 3–5 drops (0.035 ml/drop) twice daily and massage. Continue uninterrupted for several days after complete clinical resolution, at least 7 and at most 14 days; veterinary confirmation of cure is required before stopping.
  • Long or extensive corticosteroid exposure can cause local immunosuppression, secondary infection, epidermal thinning, delayed healing, telangiectasia/bleeding and systemic adrenal effects; licking and occlusion increase exposure.
  • Very rare deafness is reported, especially in older dogs. Stop for new hearing loss, head tilt, nystagmus, ataxia or severe pain and investigate otitis media/interna.
  • Ototop is only adjunctive when Otodectes cynotis coexists with susceptible secondary infection. Diagnose and treat mites with an appropriate acaricide and manage all in-contact animals/environment as indicated.
  • Do not use with hypersensitivity to miconazole, polymyxin B, prednisolone, related corticosteroids/azoles or excipients. Pregnancy/lactation safety is unestablished; use only after veterinary benefit–risk assessment and avoid mammary-gland application.
  • Treat the primary cause—commonly allergy, parasites, foreign body, conformation or endocrine disease—or recurrence is likely. Steroid-driven relief does not prove microbial eradication.
  • Shake well and prevent dropper contact with ear, skin or fingers. Wear gloves, wash hands and avoid eye/skin contact or ingestion; pregnant or breastfeeding handlers should use particular caution.
  • Do not mix with another veterinary medicine because compatibility studies are absent. Store below 25°C and discard six months after first opening; document opening date, course, susceptibility basis and recheck result.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Miconazole23 mg/ml Prednisolone5 mg/ml Polymyxin B5500 IU/ml
Formulation Type
Ear drops
Administration route
Into the ear, On the skin
Registration
Georgia Yes, veterinary
Veterinary (National Food Agency)
In the register: ოტოტოპი
Verified on: 22 Oct 2026
EU Yes, veterinary
№ DCP DE/V/0321/001; PL 3001/20; LT/2/20/2602/001–003
Verified on: 22 Oct 2026
UK No
US No
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 18 Oct 2026
Information not fully verified Shake well. Otitis: after examination, intact-tympanum confirmation and cleaning, apply 3–5 drops (0.035 ml/drop) into the external canal twice daily and massage; continue uninterrupted for several days after complete clinical resolution, at least 7 and at most 14 days, with veterinary confirmation of cure. Skin: clip/clean as needed, apply and rub in a thin film twice daily, normally up to 14 days; persistent signs may require 2–3 weeks only with repeated examination and diagnostic verification, and ongoing antifungal treatment should use no glucocorticoid when appropriate.

All of this shows in vetman as you prescribe

The dose for the patient's weight, registration in Georgia and controlled status, right on the prescription.