FDA label d61d279c-8497-b418-e053-2995a90a3cc9

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
fbf6b4d1-9bb1-493d-ae43-5e8a491cbc24
SPL ID
d61d279c-8497-b418-e053-2995a90a3cc9
Version
7
Effective date
2022-01-21
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:22:59

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. 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 AGAIN. AVOID USE ON DEEP PUNCTURE WOUNDS ANIMAL BITES OR SERIOUS BURNS.

Reported adverse events (FAERS/openFDA)#

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