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Mupirocin

Mupirocin cream is indicated for the treatment of secondarily infected traumatic skin lesions (up to 10 cm in length or 100 cm 2 in area) due to susce.

Prescription medicine Topical Safety alerts on record

How to use Mupirocin

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

Mupirocin cream is indicated for the treatment of secondarily infected traumatic skin lesions (up to 10 cm in length or 100 cm 2 in area) due to susceptible isolates of Staphylococcus aureus (S. aureus) and Streptococcus pyogenes (S. pyogenes) . Mupirocin cream is an RNA synthetase inhibitor antibacterial indicated for the treatment of secondarily infected traumatic skin lesions (up to 10 cm in length or 100 cm 2 in area) due to susceptible isolates of Staphylococcus aureus and Streptococcus pyogenes . ( 1 )

Comment le prendre et à quelle fréquence
  • For Topical Use Only
  • Apply a small amount of mupirocin cream, with a cotton swab or gauze pad, to the affected area 3 times daily for 10 days
  • Cover the treated area with gauze dressing if desired
  • Re-evaluate patients not showing a clinical response within 3 to 5 days
  • Mupirocin cream is not for intranasal, ophthalmic, or other mucosal use [see Warnings and Precautions ]
  • Do not apply mupirocin cream concurrently with any other lotions, creams or ointments [see Clinical Pharmacology ]
  • For Topical Use Only
  • Apply a small amount of mupirocin cream, with a cotton swab or gauze pad, to the affected area 3 times daily for 10 days
  • Re-evaluate patients not showing a clinical response within 3 to 5 days
  • Not for intranasal, ophthalmic, or other mucosal use
Strengths it comes in

Mupirocin cream USP, 2% is a white to off white cream that contains 20 mg (2% w/w) of mupirocin per gram in an oil-and water-based emulsion, supplied in 15-gram and 30-gram tubes. Cream: 20 mg (2% w/w) of mupirocin per gram in 15-gram and 30-gram tubes. ( 3 )

Children
  • The safety and effectiveness of mupirocin cream have been established in the age-groups 3 months to 16 years
  • Use of mupirocin cream in these age-groups is supported by evidence from adequate and well‑controlled trials of mupirocin cream
  • In adults with additional data from 93 pediatric subjects studied as part of the pivotal trials
  • In adults [see Clinical Studies ]
Older adults

In 2 adequate and well‑controlled trials, 30 subjects older than 65 years were treated with mupirocin cream. No overall difference in the efficacy or safety of mupirocin cream was observed in this patient population when compared with that observed in younger patients.

While you are taking it
  • Advise the patient to read the FDA-approved patient labeling (Patient Information)
  • Advise the patient to administer mupirocin cream as follows: Use mupirocin cream only as directed by the healthcare provider
  • It is for external use only
  • Avoid contact of mupirocin cream with the eyes
  • If mupirocin cream gets in the eyes, rinse thoroughly with water
  • Do not use mupirocin cream in the nose
  • Wash your hands before and after applying mupirocin cream
  • Use a gauze pad or cotton swab to apply a small amount of mupirocin cream to the affected area
  • The treated area may be covered by gauze dressing if desired
  • Report to the healthcare provider any signs of local adverse reactions. …
Talk to a doctor first if
  • Mupirocin cream is contraindicated in patients with known hypersensitivity to mupirocin or any of the excipients of mupirocin cream
  • Known hypersensitivity to mupirocin or any of the excipients of mupirocin cream
Warnings

Severe Allergic Reactions: Anaphylaxis, urticaria, angioedema, and generalized rash have been reported in patients treated with formulations of mupirocin, including mupirocin cream. ( 5.1 ) Eye Irritation: Avoid contact with eyes. ( 5.2 ) Local Irritation: Discontinue in the event of sensitization or severe local irritation. ( 5.3 ) Clostridium difficile -Associated Diarrhea (CDAD): If diarrhea occurs, evaluate patients for CDAD. ( 5.4 ) Potential for Microbial Overgrowth: Prolonged use may result in overgrowth of nonsusceptible microorganisms, including fungi. ( 5.5 ) Risk Associated with Mucosal Use: Mupirocin cream is not formulated for use on mucosal surfaces. …

Effets secondaires possibles

The following adverse reactions are discussed in more detail in other sections of the labeling: Severe Allergic Reactions [see Warnings and Precautions ( 5.1 )] Eye Irritation [see Warnings and Precautions ( 5.2 )] Local Irritation [see Warnings and Precautions ( 5.3 )] Clostridium difficile -Associated Diarrhea [see Warnings and Precautions ( 5.4 )] The most frequent adverse reactions (at least 1%) were headache, rash, and nausea. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary There are insufficient human data to establish whether there is a drug-associated risk with mupirocin cream in pregnant women. Systemic absorption of mupirocin through intact human skin is minimal following topical administration of mupirocin cream [see Clinical Pharmacology ( 12.3 )] . …

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-03-18.

Marques dans le monde

Products with Mupirocin as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

MupirocinMUPIROCIN CALCIUM 20 mg/g · Cream · Sun Pharmaceutical Industries, Inc.
NDC 51672-1370Label
MupirocinMUPIROCIN CALCIUM 2 g/100g · Cream · Encube Ethicals, Inc.
NDC 21922-029Label
MupirocinMUPIROCIN 20 mg/g · Ointment · Sun Pharmaceutical Industries, Inc.
NDC 51672-1312Label
MupirocinMUPIROCIN 20 mg/g · Ointment · NuCare Pharmaceuticals,Inc.
NDC 68071-4321Label
MupirocinMUPIROCIN 10 kg/10kg · Powder · Concord Biotech Limited
NDC 68254-0010Label

Nigeria (NAFDAC)

NAFDACMupirocin Ointment A4-100733NAFDACMupirocin Ointment USP 2% w/w A4-100451NAFDACMupirocin Ointment USP 2.0% w/w_ A4-101637NAFDACMytar 15 g A4-100656NAFDACMacroban Cream A11-100574NAFDACBotigo Ointment A4-101101NAFDACRovisk Ointment C4-1887NAFDACMupiderm Ointment B4-2835NAFDACMupisoft Ointment_ A4-101740NAFDACNorbaderm Ointment A4-100742NAFDACSupirocin Ointment 04-7547NAFDACBactrox 20 mg Ointment A4-101001

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

Mupirocin Ointment, USP, 2%, 22 g, Rx only, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USAU.S. FDA Class II
30 Aug 2024 · Glenmark Pharmaceuticals Inc., USA · CompletedSubpotent Drug
Mupirocin Ointment, USP 2%, 22 grams tube, Rx only, MFG: Teva Pharma USA, NDC 0093-1010-42, MFG: Teva Pharma USAU.S. FDA Class II
13 Apr 2022 · Mckesson Medical-Surgical Inc. Corporate Office · TerminatedcGMP deviations: Temperature abuse
Bactroban Cream, (Mupirocin Calcium Cream 2%), 15 gram tube, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709, Made in England, NDC 0029-1527-22,U.S. FDA Class II
18 Jul 2016 · GlaxoSmithKline, LLC · TerminatedPenicillin Cross Contamination
Bactroban Ointment, (Mupirocin Ointment 2%), 22 gram tube, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709, Made in England, NDC 0029-1525-44,U.S. FDA Class II
18 Jul 2016 · GlaxoSmithKline, LLC · TerminatedPenicillin Cross Contamination

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Mupirocin

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Questions about Mupirocin

What is Mupirocin used for?

Mupirocin cream is indicated for the treatment of secondarily infected traumatic skin lesions (up to 10 cm in length or 100 cm 2 in area) due to susceptible isolates of Staphylococcus aureus (S. aureus) and Streptococcus pyogenes (S. pyogenes) . Mupirocin cream is an RNA synthetase inhibitor antibacterial indicated for the treatment of secondarily infected traumatic skin lesions (up to 10 cm in length or 100 cm 2 in (From the official U.S. FDA label.)

How do I take Mupirocin?

Follow your prescription or the leaflet in your pack. The official label says: For Topical Use Only. Apply a small amount of mupirocin cream, with a cotton swab or gauze pad, to the affected area 3 times daily for 10 days. Cover the treated area with gauze dressing if desired. Re-evaluate patients not showing a clinical response within 3 to 5 days. Mupirocin cream is not for intranasal, ophthalmic, or other mucosal use [see Warnings and Precautions ( 5.2 …

Do I need a prescription for Mupirocin?

Usually yes. Mupirocin is a prescription medicine in most countries. Rules differ by country.

What brands contain Mupirocin?

Mupirocin is sold under names such as Muricin, Bactroban, Pirnuo, Centany, Mupirocin. Brand names differ between countries.

How can I check that my Mupirocin is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.