FDA label fcbbd362-c5c2-42b2-99f5-b0585aaa9602

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
4a735a5b-98cd-4dc1-a10d-0493fd4b1e21
SPL ID
fcbbd362-c5c2-42b2-99f5-b0585aaa9602
Version
3
Effective date
2018-12-27
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:54

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 use more than instructed. When using Avoid the eye area must close the cap after using

Reported adverse events (FAERS/openFDA)#

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