FDA label 895c6940-e1a5-45a9-9026-7890a5d080e8

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
c7be9522-054e-4dad-99f3-e15eb6fe84b9
SPL ID
895c6940-e1a5-45a9-9026-7890a5d080e8
Version
1
Effective date
2017-01-20
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 06:31:38

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 Warnings: If the following signs occur please stop using immediately and consult a dermatologist. stop using if skin becomes red, swollen, itchy and etc during and after use. Avoid using on irritated or sunburned skin by direct sunlight. For areas with infection or high inflammatory activity, do not use. Storage and Handling Precautions. Put the lid back on after you have used it. Keep away from the reach of baby and children. Do not keep places of the high temperature or low temperature and direct sunlight.

Reported adverse events (FAERS/openFDA)#

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