Neomycin
Minaderm Pomade · ATC code D06AX04
Also known as: Neomisin, Neomycin Sulfate
- Key facts
- Active substance
- Neomycin
- ATC code
- D06AX04
- Authorisation
- authorised nationally; no central EU authorisation
- Information as of
- 2026-10-29
Boxed warning
SYSTEMIC ABSORPTION OF NEOMYCIN OCCURS FOLLOWING ORAL ADMINISTRATION AND TOXIC REACTIONS MAY OCCUR. Patients treated with neomycin should be under close clinical observation because of the potential toxicity associated with their use. NEUROTOXICITY (INCLUDING OTOTOXICITY) AND NEPHROTOXICITY FOLLOWING THE ORAL USE OF NEOMYCIN SULFATE HAVE BEEN REPORTED, EVEN WHEN USED IN RECOMMENDED DOSES. THE POTENTIAL FOR NEPHROTOXICITY, PERMANENT BILATERAL AUDITORY OTOTOXICITY AND SOMETIMES VESTIBULAR TOXICITY IS PRESENT IN PATIENTS WITH NORMAL RENAL FUNCTION WHEN TREATED WITH HIGHER DOSES OF NEOMYCIN AND/OR FOR LONGER PERIODS THAN RECOMMENDED. Serial, vestibular and audiometric tests, as well as tests of renal function, should be performed (especially in high-risk patients). THE RISK OF NEPHROTOXICITY AND OTOTOXICITY IS GREATER IN PATIENTS WITH IMPAIRED RENAL FUNCTION. Ototoxicity is often delayed in onset and patients developing cochlear damage will not have symptoms during therapy to warn them of developing eighth nerve destruction and total or partial deafness may occur long after neomycin has been discontinued.
Neuromuscular blockage and respiratory paralysis have been reported following the oral use of neomycin. The possibility of the occurrence of neuromuscular blockage and respiratory paralysis should be considered if neomycin is administered, especially to patients receiving anesthetics, neuromuscular blocking agents such as tubocurarine, succinylcholine, decamethonium, or in patients receiving massive transfusions of citrate anticoagulated blood. If blockage occurs, calcium salts may reverse these phenomena but mechanical respiratory assistance may be necessary.
Concurrent and/or sequential systemic, oral or topical use of other aminoglycosides, including paromomycin and other potentially nephrotoxic and/or neurotoxic drugs such as bacitracin, cisplatin, vancomycin, amphotericin B, polymyxin B, colistin and viomycin, should be avoided because the toxicity may be additive.
Other factors which increase the risk of toxicity are advanced age and dehydration.
The concurrent use of neomycin with potent diuretics such as ethacrynic acid or furosemide should be avoided, since certain diuretics by themselves may cause ototoxicity. In addition, when administered intravenously, diuretics may enhance neomycin toxicity by altering the antibiotic concentration in serum and tissue.
Key facts
Neomycin is an aminoglycoside antibiotic, here as oral tablets. Per the US prescribing information, it is used to suppress intestinal bacteria before bowel surgery and as adjunctive therapy in hepatic coma.
What it is used for
- Suppression of the normal bowel flora, e.g. preoperative bowel preparation, together with enteric-coated erythromycin
- Adjunctive therapy in hepatic coma (portal-systemic encephalopathy), by reducing ammonia-forming intestinal bacteria
Dosing
- Use the lowest possible dose for the shortest possible time; treatment longer than two weeks is not recommended
- Hepatic coma: 4 to 12 grams per day in divided doses for five to six days, with protein withdrawn from the diet and diuretics avoided
- Chronic hepatic insufficiency: up to four grams daily may be necessary if less toxic drugs cannot be used; frequent monitoring including serum neomycin levels is mandatory
- Preoperative bowel preparation: neomycin 1 g with erythromycin base 1 g orally, three doses on the day before surgery – see the full text for the full schedule
Contraindications
- Intestinal obstruction
- Hypersensitivity to neomycin (cross-sensitivity with other aminoglycosides possible)
- Inflammatory or ulcerative gastrointestinal disease
Important warnings
- Boxed warning: systemic absorption after oral use; neurotoxicity (including ototoxicity) and nephrotoxicity, even at recommended doses; risk greater with impaired renal function; hearing loss may appear long after stopping
- Serial vestibular, audiometric and renal function tests should be performed
- Neuromuscular blockage and respiratory paralysis, especially with anesthetics or neuromuscular blocking agents
- Aminoglycosides can cause fetal harm
- Increased risk of ototoxicity in patients with certain mitochondrial DNA variants
Side effects
- Most common: nausea, vomiting and diarrhea
- Malabsorption syndrome with prolonged therapy
- Serious: nephrotoxicity, ototoxicity, neuromuscular blockage; numbness, skin tingling, muscle twitching, convulsions
Interactions
- Other aminoglycosides (including paromomycin) and other nephrotoxic or neurotoxic drugs: avoid
- Potent diuretics such as ethacrynic acid or furosemide: avoid
- Digoxin absorption may be reduced – monitor levels; may enhance the effect of coumarin anticoagulants
- Absorption of vitamin B-12, methotrexate and 5-fluorouracil may be reduced
Pregnancy and breastfeeding
- Aminoglycosides cross the placenta and can cause fetal harm; congenital deafness has been reported with streptomycin
Summary of the official product information, written with AI on 2026-10-29. Every number was checked automatically against the original text. Not reviewed by a physician – the full official text is authoritative.
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For patients
Patient information (US)
This product has no separate US patient information.
Authorisation and brand names by country
Medicines with exactly this active-substance composition, as listed in the national registers – alphabetical and without ranking. Whether a product is currently available is not shown here.
Germany
- MyacyneMaxmedic Pharma Gmbh. · 1 register entry
- Neomycinsulfat Smartpractice EuropeSmartpractice Europe Gmbh · 1 register entry
Source: EMA – Article 57 product data (EU/EEA), as of 2026-10-29
Turkey
- Minaderm PomadeGÜNSA GÜNEY İLAÇ VE HAMMADDELER SAN. VE TİC. A.Ş. · 1 register entry
Source: TİTCK – Ruhsatlı Beşeri Tıbbi Ürünler Listesi, as of 2026-10-16
Brand names in 3 more European countries
- Poland
- Neobiotic, Neomycinum, Unguentum, Неомицинум Tc
- Portugal
- Neomicina Labesfal
- Spain
- Neomicina
EMA – Article 57 product data (EU/EEA), 2026-10-29
Medelix receives no money from pharmaceutical companies. Brand names are listed alphabetically and without ranking.
Another question about this substance?
Medelix answers clinical questions from guidelines, studies and product information – every claim with its source.
Sources
- U.S. Food and Drug Administration. Neomycin Sulfate (Chartwell RX, LLC) – Prescribing Information, 2026-02-27. DailyMed (NLM), 2026-10-29. https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0aa6947b-4739-4b00-be93-7303a5fc687d
- EMA – Article 57 product data (EU/EEA), 2026-10-29. https://www.ema.europa.eu/en/human-regulatory-overview/post-authorisation/data-medicines-iso-idmp-standards-post-authorisation/public-data-article-57-database
- TİTCK – Ruhsatlı Beşeri Tıbbi Ürünler Listesi, 2026-10-16. https://www.titck.gov.tr/dinamikmodul/85
Editorial: Medelix editorial team · last updated 2026-10-29 · How these pages are made · Report an error
Source: U.S. Food and Drug Administration (FDA), prescribing information, via DailyMed (NLM); public domain. Not advertising, not a treatment recommendation. For questions about your own treatment, ask your doctor or pharmacist.