FDA.reportPublic FDA data

FDA label 2cdc6fe0-ff73-4ecb-9ecb-b4e0f1f5a30d

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
15f1fbce-1e13-44b3-b204-9f43bd4c58af
SPL ID
2cdc6fe0-ff73-4ecb-9ecb-b4e0f1f5a30d
Version
3
Effective date
2019-03-26
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:51

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.