FDA label 0e847aaa-54b6-47bb-9337-5cdeaf45761b

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
575fbe21-edff-40e5-9a56-660f6b0e0a8c
SPL ID
0e847aaa-54b6-47bb-9337-5cdeaf45761b
Version
1
Effective date
2018-08-30
Source export date
2026-11-06
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:43:48

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. Discontinue use immediately and consult a dermatologist, if you experience the following: 1) Irritation, Red spots, itchy skin or rash 2) Applied skin area has the above reaction from direct sun 2. Do not use on irritated skin, cuts, or other infected skin area. 3. Avoid contact with eyes. 4. close the cap after using. 5. keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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