FDA label 07e67720-4735-c363-e063-6394a90ae9a2

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
07e6bbce-c06c-559a-e063-6394a90a52a3
SPL ID
07e67720-4735-c363-e063-6394a90ae9a2
Version
1
Effective date
2023-10-17
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:24:17

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 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.