FDA label 316f56f2-e853-44b3-e054-00144ff8d46c

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
316f56f2-e852-44b3-e054-00144ff8d46c
SPL ID
316f56f2-e853-44b3-e054-00144ff8d46c
Version
1
Effective date
2016-04-26
Source export date
2026-09-28
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/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:33:46

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

1. If rash, flare, itching, and other symptoms are caused by the treatment, then stop using it and contact a medical doctor or a pharmacist. 2. Do not apply on skin regions with damage, eczema and dermatitis. 3. If it goes in the eyes, immediately clean the eyes. 4. Attention in storage 1) Close the lid after use. 2) Keep it away from the touch of young children. 3) Keep out of high temperature, low temperature, and direct sunlight.

Reported adverse events (FAERS/openFDA)#

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