Mupirocin
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Mupirocin
- Generic name
- MUPIROCIN
- Manufacturer
- Proficient Rx LP
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 2777e4f2-2b8d-41f5-a96a-02dec8c7c3e0
- SPL ID
- 141d8892-7f38-43d4-8bc4-5a0bf6198717
- Version
- 4
- Effective date
- 2023-11-01
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:07:05
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 090480 | derived:openfda.application_number |
| application number | ANDA090480 | openfda.application_number | |
| brand name | Mupirocin | openfda.brand_name | |
| generic name | MUPIROCIN | openfda.generic_name | |
| manufacturer name | Proficient Rx LP | openfda.manufacturer_name | |
| ndc | package | 63187-015-22 | openfda.package_ndc |
| ndc | product | 63187-015 | openfda.product_ndc |
| ndc11 | package | 63187001522 | derived:openfda.package_ndc |
| rxcui | 106346 | openfda.rxcui | |
| spl id | 141d8892-7f38-43d4-8bc4-5a0bf6198717 | id | |
| spl set id | 2777e4f2-2b8d-41f5-a96a-02dec8c7c3e0 | set_id | |
| unii | D0GX863OA5 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS Mupirocin ointment is not for ophthalmic use.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS The following local adverse reactions have been reported in connection with the use of mupirocin ointment : Burning, stinging, or pain in 1.5% of patients; itching in 1% of patients; rash, nausea, erythema, dry skin, tenderness, swelling, contact dermatitis, and increased exudate in less than 1% of patients. Systemic reactions to mupirocin ointment have occurred rarely.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.