FDA label c47959fc-0fb3-31c0-e053-2995a90a4f21

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
29bae596-3b2e-46b7-afef-b50b304f1811
SPL ID
c47959fc-0fb3-31c0-e053-2995a90a4f21
Version
5
Effective date
2021-06-11
Source export date
2026-11-06
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:52:22

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)After or while using the cosmetic product, if redness, swelling, itchiness, or any other similar symptom or discomfort arises upon contact with direct sunline, please consult a healthcare provider before using any further 2)Avoid using on wounded areas 3)Important notes for storage and handling a) Store at places where children cannot reach b) Store at places with no direct sunlight 4)Avoid contact with eye

Reported adverse events (FAERS/openFDA)#

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