FDA label b1fd144a-f6e9-4898-8b28-704d449e4e15

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 (canonical bytes are SHA-256 checked before publication)

SPL set ID
34a8bf10-1c18-1c14-e063-6394a90a0a6f
SPL ID
b1fd144a-f6e9-4898-8b28-704d449e4e15
Version
5
Effective date
2025-05-08
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:29:44

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only Do not use: In the eyes, nose, mouth, or on large areas of the body If you are allergic to mupirocin or any of the ingredients in this product Ask a doctor before use if you have: Deep or puncture wounds Animal bites Serious burns Large areas of damaged skin ■ Avoid contact with eyes. If contact occurs, rinse thoroughly with water. ■ Use only as directed. Do not use for longer than prescribed. ■ Do not bandage tightly unless directed by a doctor. Stop use and ask a doctor if Condition worsens or does not improve within 3-5 days Rash,irritation, or other allergic reaction develops If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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