FDA label 07831e0d-c839-7153-e063-6394a90a8b7a

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
0782c8ff-36e8-f0ac-e063-6294a90aa87b
SPL ID
07831e0d-c839-7153-e063-6394a90a8b7a
Version
1
Effective date
2023-10-12
Source export date
2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:09:59

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 notreplace 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.