FDA label 44f0d9b3-64e2-4204-a163-7f39a72fb09c

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
e9904185-e075-4181-9498-f7cd095a6139
SPL ID
44f0d9b3-64e2-4204-a163-7f39a72fb09c
Version
1
Effective date
2020-03-30
Source export date
2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:37:31

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.