FDA label 07e7b8d1-4609-4926-e063-6394a90aa72c

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
07e7b8d1-4608-4926-e063-6394a90aa72c
SPL ID
07e7b8d1-4609-4926-e063-6394a90aa72c
Version
1
Effective date
2023-10-17
Source export date
2026-11-06
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:39:54

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.Stop use and ask doctor if rash occurs.Keep out reach of children. Precautions 1. This product is an external product,do not take it internally; 2. This product is a disposable external product,not a substitute for drugs or medical equipment;Do not reuse it; 3. Pregnant women,infants,breastfeeding,and those allergic to this product are prohibited; 4. Do not use skin allergies,skin damage,skin diseases and other symptoms; 5. If the skin appears red,itchy and other abnormal conditions during use,please suspend use.

Reported adverse events (FAERS/openFDA)#

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