FDA label 4851a7ce-5d4e-861c-e063-6394a90aa539

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
26365925-ee30-aa63-e063-6394a90a7f5c
SPL ID
4851a7ce-5d4e-861c-e063-6394a90aa539
Version
4
Effective date
2026-01-13
Source export date
2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:55:03

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 1. This product is for external use, should not be applied to the face, do not take internally. 2. Do not use if you have skin allergies, broken skin or skin diseases. 3. Pregnant women, infants, lactation, allergic to the product is prohibited. 4. This product can not be uised as a substitute for drugs or medical devices, if there are special circumstances, please follow the doctor's instructions. 5. If skin redness, itching and other abnormal conditions occur during use, please suspend use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.