FDA label d559a120-8e23-9573-e053-2995a90a42e8

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
70377898-6150-023a-e053-2a91aa0ac9b0
SPL ID
d559a120-8e23-9573-e053-2995a90a42e8
Version
2
Effective date
2022-01-11
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 05:31:21

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

If abnormal symptoms or side effects such as red spots, swelling, or itching are present in the cosmetics or in the direct sunlight after use, consult a specialist Do not use in wounded areas Precautions for storage and handling Keep out of reach of children Keep away from direct sunlight Avoid the use of eye area

Reported adverse events (FAERS/openFDA)#

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