FDA.reportPublic FDA data

FDA label d4b682c6-7465-3990-e053-2995a90aeb3f

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
2db748ee-519f-42d5-aac1-d2737d57fc93
SPL ID
d4b682c6-7465-3990-e053-2995a90aeb3f
Version
3
Effective date
2022-01-03
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:33:17

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. AVOID CONTACT WITH EYES AND MUCOUS MEMBRANES. DO NOT USE ON SENSITIVE AREAS, FACE, OR EYE AREA. IF CONDITION WORSENS, OR IF SYMPTOMS PERSIST FOR MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS, DISCONTINUE USE OF THIS PRODUCT AND CONSULT A DOCTOR. DO NOT APPLY TO WOUNDS OR DAMAGED SKIN, OR IRRITATED AREAS. DO NOT BANDAGE TIGHTLY IN THE AREA WHERE PRODUCT IS APPLIED. DO NOT USE A HEATING PAD IN AREA WHERE PRODUCT IS APPLIED.

Reported adverse events (FAERS/openFDA)#

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