FDA label 08096e9d-a5a8-446d-e063-6294a90a8047

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
08096e84-4053-75ed-e063-6294a90a9c25
SPL ID
08096e9d-a5a8-446d-e063-6294a90a8047
Version
1
Effective date
2023-10-18
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:44:14

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

Precautions 1.This product is an external product, do not take it internally; 2.This product is a health care product and does not replace drugs and medical devices for treatment; 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.