FDA label 0796ec1f-7944-60f3-e063-6294a90afc41

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
0796ec0c-e0e3-7e5b-e063-6294a90a0cf3
SPL ID
0796ec1f-7944-60f3-e063-6294a90afc41
Version
1
Effective date
2023-10-13
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:24:33

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.