FDA label 9f2617ea-ae0b-64ff-e053-2a95a90a39e0

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
9f2617d1-f693-29f8-e053-2a95a90a09cc
SPL ID
9f2617ea-ae0b-64ff-e053-2a95a90a39e0
Version
1
Effective date
2020-02-22
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:02:10

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

1. If skin develops abnormal symptoms and side effects such as red spots, swelling, and itching while using the cosmetic or after using this cosmetic, or if the application area develops the symptoms above after exposure to direct sunlight, consult your dermatologist. 2. Do not apply on areas with open wounds. 3. Storage & Handling (1) Keep out of reach of children. (2) Keep away from direct sunlight. 4. If the product get into eyes, wash off immediately with water. 5. If you do not wash off thoroughly with water after use, it may cause hair loss or discoloration.

Reported adverse events (FAERS/openFDA)#

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