FDA label d6fa3422-beaf-0772-e053-2995a90a4920

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
d60ee279-1a76-7448-e053-2995a90a6de1
SPL ID
d6fa3422-beaf-0772-e053-2995a90a4920
Version
3
Effective date
2022-02-01
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:14:17

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

WARNINGS FOR EXTERNAL USE ONLY. DO NOT USE ON DEEP OR PUNCTURE WOUNDS ON ANIMAL BITES ON SERIOUS BURNS WHEN USING THIS PRODUCT DO NOT GET INTO EYES. STOP USE AND ASK A DOCTOR IF CONDITION WORSENS SYMPTOMS LAST MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAINWITHIN A FEW DAYS.

Reported adverse events (FAERS/openFDA)#

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