FDA label d1dfc053-42fe-41c1-89be-63efd2a8886c

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
baca1368-34ca-45fd-b33f-3be503e7eafd
SPL ID
d1dfc053-42fe-41c1-89be-63efd2a8886c
Version
1
Effective date
2019-09-17
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 05:50:59

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: For external use only. If the following signs occur, please stop using immediately and consult a dermatologist. Stop using immediately if skin become red, swollen, or itchy during and after use. Avoid using on irritated of sunburnt skin. Stop using on troubled skin parts including eczema or dermatitis. Avoid direct contact with the eyes, if contact occurs, rinse eyes thoroughly with water. In order to prevent dryness, use soon after opening the package. Keep away from the reach of babies and children. Store at room temperature only. Keep away from direct sunlight.

Reported adverse events (FAERS/openFDA)#

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