FDA.reportPublic FDA data

FDA label 262175f4-6f0f-3715-e063-6394a90a46d3

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
23a12574-69f4-7198-e063-6394a90aae1c
SPL ID
262175f4-6f0f-3715-e063-6394a90a46d3
Version
2
Effective date
2024-11-04
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:33:58

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

Warnings 1. This product is for external use, avoid eyes and wound areas, open and use immediately; 2. Please place it out of reach of children to prevent accidental ingestion. 3. Due to individual differences in skin, each person has different adaptability to the product, it is recommended that before use behind the ear and the inner arm to do the skin adaptability test, such as skin irritationor discomfort, please pause the use and consult a professional dermatologist.

Reported adverse events (FAERS/openFDA)#

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