CENTANY ™ (mupirocin ointment),2%

Manufacturer
OrthoNeutrogena, Division of Ortho-McNeil Pharmaceutical, Inc.
Effective date
2007-02-13
Label type
HUMAN PRESCRIPTION DRUG LABELING
Version
1
Source
full-release
Hydrated at
2026-05-31 20:06:51

Label at a glance#

ProductCENTANY
Label structure11 sections

Indications and uses

Centany (mupirocin ointment),2% is indicated for the topical treatment of impetigo due to: Staphylococcus aureus and Streptococcus pyogenes .

Dosage and administration

A small amount of Centany (mupirocin ointment),2% should be applied to the affected area three times daily. The area treated may be covered with a gauze dressing if desired. Patients not showing a clinical response within 3 to 5 days should be re-evaluated.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

OrthoNeutrogena

Rx only       For Dermatologic Use

DESCRIPTION

DESCRIPTION SECTION

Each gram of Centany (mupirocin ointment),2% contains 20 mg mupirocin in a soft white ointment base consisting of castor oil, oleyl alcohol, hard fat (Softisan® 378) and propylene glycol monostearate. Mupirocin is a naturally occurring antibiotic. The chemical name is (E)-(2S,3R,4R,5S)-5-[(2S,3S,4S,5S)-2,3-Epoxy-5-hydroxy-4-methylhexyl]tetrahydro-3,4-dihydroxy-β-methyl-2 H-pyran-2-crotonic acid, ester with 9-hydroxynonanoic acid. The molecular formula of mupirocin is C26H44O9 and the molecular weight is 500.63. The chemical structure is:

DESCRIPTION
DESCRIPTION

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Following the application of Centany (mupirocin ointment),2% to a 400 cm2 area on the back of 23 healthy volunteers once daily for 7 days, the mean (range) cumulative urinary excretion of monic acid over 24 hrs following the last administration was 1.25% (0.2% to 3.0%) of the administered dose of mupirocin. The monic acid concentration in urine collected at specified intervals for 24 hrs on Day 7 ranged from <0.050 to 0.637 μg/mL.

SPL UNCLASSIFIED SECTION

Microbiology: Mupirocin is an antibacterial agent produced by fermentation using the organism Pseudomonas fluorescens. Its spectrum of activity includes gram-positive bacteria. It is also active, in vitro only, against certain gram-negative bacteria. Mupirocin inhibits bacterial protein synthesis by reversibly and specifically binding to bacterial isoleucyl transfer-RNA synthetase. Due to this unique mode of action, mupirocin does not demonstrate cross-resistance with other classes of antimicrobial agents.

When mupirocin resistance occurs, it results from the production of a modified isoleucyl-tRNA synthetase or the acquisition, by genetic transfer, of a plasmid mediating a new isoleucyl-tRNA synthetase. High-level plasmid-mediated resistance (MIC > 500 mcg/mL) has been reported in increasing numbers of isolates of Staphylococcus aureus and with higher frequency in coagulase-negative staphylococci. Methicillin resistance and mupirocin resistance commonly occur together in Staphylococcus aureus and coagulase negative staphylococci.

Mupirocin is bactericidal at concentrations achieved by topical administration. However, the minimum bactericidal concentration (MBC) against relevant pathogens is generally eight-fold to thirty-fold higher than the minimum inhibitory concentration (MIC). In addition, mupirocin is highly protein bound (>97%), and the effect of wound secretions on the MICs of mupirocin has not been determined.

Mupirocin has been shown to be active against susceptible strains of Staphylococcus aureus and Streptococcus pyogenes, both in vitro and in clinical studies. (See INDICATIONS AND USAGE.)

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Centany (mupirocin ointment),2% is indicated for the topical treatment of impetigo due to: Staphylococcus aureus and Streptococcus pyogenes.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

This drug is contraindicated in individuals with a history of sensitivity reactions to any of its components.

WARNINGS

WARNINGS SECTION

Centany (mupirocin ointment),2% is not for ophthalmic use.

PRECAUTIONS

PRECAUTIONS SECTION

If a reaction suggesting sensitivity or chemical irritation should occur with the use of Centany (mupirocin ointment),2%, treatment should be discontinued and appropriate alternative therapy for the infection instituted.

As with other antibacterial products, prolonged use may result in overgrowth of nonsusceptible organisms, including fungi. Centany (mupirocin ointment),2% is not formulated for use on mucosal surfaces. Centany (mupirocin ointment),2% is not intended for nasal use.

INFORMATION FOR PATIENTS SECTION

Information for Patients: Use this medication only as directed by your healthcare provider. It is for external use only. Avoid contact with the eyes. The medication should be stopped and your healthcare practitioner contacted if irritation, severe itching or rash occurs. If impetigo has not improved in 3 to 5 days, contact your healthcare practitioner.

DRUG INTERACTIONS SECTION

Drug Interactions: The effect of the concurrent application of Centany (mupirocin ointment),2% and other drug products is unknown.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Carcinogenesis, Mutagenesis, Impairment of Fertility: Long-term studies in animals to evaluate carcinogenic potential of mupirocin have not been conducted.

Results of the following studies performed with mupirocin calcium or mupirocin sodium in vitro and in vivo did not indicate a potential for genotoxicity: rat primary hepatocyte unscheduled DNA synthesis, sediment analysis for DNA strand breaks, Salmonella reversion test (Ames), Escherichia coli mutation assay, metaphase analysis of human lymphocytes, mouse lymphoma assay, and bone marrow micronuclei assay in mice.

Reproduction studies were performed in male and female rats with mupirocin administered subcutaneously at doses up to 14 times the human topical dose (approximately 60 mg mupirocin/ day) on a mg/m2 basis and revealed neither evidence of impaired fertility nor impaired reproductive performance attributable to mupirocin.

Pregnancy

Teratogenic Effects.

TERATOGENIC EFFECTS SECTION

SPL UNCLASSIFIED SECTION

Pregnancy Category B: Reproduction studies have been performed in rats and rabbits with mupirocin administered subcutaneously at doses up to 22 and 43 times, respectively, the human topical dose (approximately 60 mg mupirocin per day) on a mg/m2 basis and revealed no evidence of harm to the fetus due to mupirocin. There are, however, no adequate and well-controlled studies in pregnant women. Because animal studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

NURSING MOTHERS SECTION

Nursing Mothers: It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Centany (mupirocin ointment),2% is administered to a nursing woman.

PEDIATRIC USE SECTION

Pediatric Use: The safety and effectiveness of Centany (mupirocin ointment),2% have been established in the age range of 2 months to 16 years. Use of Centany (mupirocin ointment),2% in these age groups is supported by evidence from adequate and well-controlled studies of Centany (mupirocin ointment),2% in impetigo in pediatric patients studied as a part of the pivotal clinical trials. (See CLINICAL STUDIES.)

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

The following local adverse reactions have been reported in connection with the use of Centany (mupirocin ointment),2%; application site reactions and pruritus, each in 1% of patients; contact dermatitis and furunculosis, each in 0.7% of patients; and exfoliative dermatitis and rash, each in 0.3% of patients.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

A small amount of Centany (mupirocin ointment),2% should be applied to the affected area three times daily. The area treated may be covered with a gauze dressing if desired. Patients not showing a clinical response within 3 to 5 days should be re-evaluated.

CLINICAL STUDIES

CLINICAL STUDIES SECTION

The efficacy of topical Centany (mupirocin ointment),2% in impetigo was tested in one study. Patients with impetigo were randomized to receive either Centany (mupirocin ointment), 2% or Bactroban® Ointment (mupirocin ointment, 2%) t.i.d. for 7 days. Clinical efficacy rates at the follow-up visit (one week after end of therapy) in the evaluable populations (adults and pediatric patients included) were 94% for Centany (mupirocin ointment), 2% (n=233) and 95% for Bactroban® Ointment (mupirocin ointment, 2%) (n=242). Pathogen eradication rates at follow-up for both medications were 98%.

Pediatrics

SPL UNCLASSIFIED SECTION

There were 413 pediatric patients aged 2 months to 15 years in the clinical study described above. Clinical efficacy rates at follow-up in the evaluable populations were 93% for Centany (mupirocin ointment), 2% (n=199) and 95% for Bactroban® Ointment (mupirocin ointment, 2%) (n=214).

HOW SUPPLIED

HOW SUPPLIED SECTION

Centany (mupirocin ointment),2% is supplied in 15 gram (NDC 0062-1610-01) and 30 gram (NDC 0062-1610-03) tubes.

Store at controlled room temperature 20° to 25°C (68° to 77°F).

OrthoNeutrogena

Distributed by: OrthoNeutrogena, Division of Ortho-McNeil Pharmaceutical, Inc.
Skillman, New Jersey 08558
©OMP 2004
Rev: April 2004
Printed in USA
635-10-686-3
U.S. Patent No. 6,013,657

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
404070CENTANY 2 % Topical OintmentPSN1
106346mupirocin 2 % Topical OintmentPSN1
404070mupirocin 0.02 MG/MG Topical Ointment [Centany]SBD1
106346mupirocin 0.02 MG/MG Topical OintmentSCD1
404070Centany 0.02 MG/MG Topical OintmentSY1
404070Centany 2 % Topical OintmentSY1
106346mupirocin 2 % Topical OintmentSY1
106346mupirocin 20 MG per GM Topical OintmentSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MUPIROCIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f2f8c312-f164-6104-0de4-ec45484840e3Product name220260304
0c2e0212-b823-4ce8-611e-853ac2cac1b2Product name420230327
3db2f5c1-f78c-f062-515c-4827e36c2518Product name120140508
f74f326b-f453-01a0-e7e7-ce5ea9475503Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0062-1610-01CENTANY15 g in 1 TUBEOINTMENT151
0062-1610-03CENTANY30 g in 1 TUBEOINTMENT301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0062-1610CENTANY (MUPIROCIN) OINTMENT [ORTHONEUTROGENA, DIVISION OF ORTHO-MCNEIL PHARMACEUTICAL, INC.]12 package rows20070216_ae3defca-06d5-49ac-8a27-be5c4e9304d1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
mupirocinACTIVE INGREDIENTD0GX863OA51
mupirocinACTIVE MOIETYD0GX863OA51
Castor oilINACTIVE INGREDIENT1
Hard fat (Softisan 378)INACTIVE INGREDIENT1
Oleyl alcoholINACTIVE INGREDIENT1
Propylene glycol monostearateINACTIVE INGREDIENT1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0062-16100062-1610-01, 0062-1610-03

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 27 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Oleyl alcoholOLEYL ALCOHOL172F2WN8DVSYSTEM / TRANSDERMAL6.12 mgName fallback — name candidate
7 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GGEL / NASAL429 mgName fallback — name candidate
16 equally ranked IID candidates
Oleyl alcoholOLEYL ALCOHOL172F2WN8DVLOTION / TOPICAL11700 mgName fallback — name candidate
7 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GTABLET / ORAL17 mgName fallback — name candidate
16 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GTABLET, COATED / ORAL0.9 mgName fallback — name candidate
16 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GEMULSION / OPHTHALMIC32 mgName fallback — name candidate
16 equally ranked IID candidates
Oleyl alcoholOLEYL ALCOHOL172F2WN8DVOINTMENT / TOPICAL5 %w/wName fallback — name candidate
7 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GTABLET / SUBLINGUAL1.6 mgName fallback — name candidate
16 equally ranked IID candidates
Oleyl alcoholOLEYL ALCOHOL172F2WN8DVFILM, EXTENDED RELEASE / TRANSDERMAL7.45 mgName fallback — name candidate
7 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GINJECTION / INTRAMUSCULAR885 mgName fallback — name candidate
16 equally ranked IID candidates
Oleyl alcoholOLEYL ALCOHOL172F2WN8DVGEL / TOPICAL150 mgName fallback — name candidate
7 equally ranked IID candidates
Propylene glycol monostearatePROPYLENE GLYCOL MONOSTEARATEMZM1I680W0CREAM / TOPICAL257 mgName fallback — name candidate
4 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GSPRAY / NASALNAName fallback — name candidate
16 equally ranked IID candidates
Oleyl alcoholOLEYL ALCOHOL172F2WN8DVGEL / TRANSDERMAL1.5 %w/wName fallback — name candidate
7 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GTABLET, DELAYED RELEASE / ORAL0.01 mgName fallback — name candidate
16 equally ranked IID candidates
Propylene glycol monostearatePROPYLENE GLYCOL MONOSTEARATEMZM1I680W0CREAM / VAGINAL140 mgName fallback — name candidate
4 equally ranked IID candidates
Oleyl alcoholOLEYL ALCOHOL172F2WN8DVCREAM / TOPICAL10 %w/wName fallback — name candidate
7 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wName fallback — name candidate
16 equally ranked IID candidates
Propylene glycol monostearatePROPYLENE GLYCOL MONOSTEARATEMZM1I680W0OINTMENT / TOPICAL8 %w/wName fallback — name candidate
4 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GINJECTION, SOLUTION / INTRAMUSCULAR525 mgName fallback — name candidate
16 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GTABLET, FILM COATED / ORAL15.29 mgName fallback — name candidate
16 equally ranked IID candidates
Propylene glycol monostearatePROPYLENE GLYCOL MONOSTEARATEMZM1I680W0LOTION / TOPICAL60 mgName fallback — name candidate
4 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GCAPSULE, EXTENDED RELEASE / ORAL47 mgName fallback — name candidate
16 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wName fallback — name candidate
16 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GCAPSULE / ORAL1.04 mgName fallback — name candidate
16 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GGRANULE, FOR SUSPENSION / ORAL128 mgName fallback — name candidate
16 equally ranked IID candidates
Castor oilCASTOR OILD5340Y2I9GTABLET, EXTENDED RELEASE / ORAL23.27 mgName fallback — name candidate
16 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2A608591-E6B9-F6BE-9870-BFB5DFEE47EDae3defca-06d5-49ac-8a27-be5c4e9304d12007-02-13Warnings, Adverse reactionsExact identifier
spl id: 2A608591-E6B9-F6BE-9870-BFB5DFEE47ED
spl set id: ae3defca-06d5-49ac-8a27-be5c4e9304d1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.