FDA label 0873e52c-3e77-e9bb-e063-6394a90a7c79

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
0873e52c-3e76-e9bb-e063-6394a90a7c79
SPL ID
0873e52c-3e77-e9bb-e063-6394a90a7c79
Version
1
Effective date
2023-10-24
Source export date
2026-10-30
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:26:58

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 fortreatment; 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.