FDA.reportPublic FDA data

FDA label 0c6f2740-1845-4b7c-8970-5d0f7db5eebf

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
d87a5388-7fa7-44bb-bcff-35d564efd820
SPL ID
0c6f2740-1845-4b7c-8970-5d0f7db5eebf
Version
3
Effective date
2020-03-03
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 02:35:24

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: Stop use and ask dermatologist or doctor if •signs of redness, skin swelling, itchy spots, irritation or rash and other appear •the above signs appear in the applied area by direct rays of the sun Do not use over •wounds rashes inflammations other troubled areas. Do not stay too long in the sun, even while using a sunscreen product. When using •Avoid the eye area •must close the cap after using Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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