FDA label fcc8ab2d-0e7e-482b-bf2c-ebf6a389e3ed

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
6eb9491a-d827-4547-acaa-9cfbb3b17f77
SPL ID
fcc8ab2d-0e7e-482b-bf2c-ebf6a389e3ed
Version
1
Effective date
2015-03-26
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:50:12

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 Warnings: 1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist. 1) red spot, swelling, itching, stimulus 2) symptoms mentioned above are caused by sunlight. 2. Do not apply on skin where there is wound, eczema, or irritation. 3. Beware of the product getting into eye. 4. Do not use for the purpose other than indicated. 5. Storage and cautions for handling 1) keep out of reach of children. 2) keep away from high or low temperature and direct sunlight.

Reported adverse events (FAERS/openFDA)#

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