FDA label f9e372bb-613f-4d9d-ae4f-cbbcc61ec949

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
e016118d-2c73-45ce-bbd3-d817944ef3b5
SPL ID
f9e372bb-613f-4d9d-ae4f-cbbcc61ec949
Version
2
Effective date
2021-06-21
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:15

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. For external use only 2. Keep out of reach of children 3. If sympoms such as redness, swelling, itching or irritation occur by being exposed to direct sunlight during or after using cosmetics, consult a doctor. 4. Not to be applied over wound 5. Test the product by placing a small amount on the inside of your elbow and waiting 24 hours to see any skin reactions.

Reported adverse events (FAERS/openFDA)#

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