FDA label 07e73716-3090-8f0f-e063-6394a90a532e

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
07e6f18d-0811-f49a-e063-6294a90a0aff
SPL ID
07e73716-3090-8f0f-e063-6394a90a532e
Version
1
Effective date
2023-10-17
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:03:43

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.