FDA label 211625cc-0d51-9f5d-e063-6294a90a9341

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
2018a9be-59d2-0d99-e063-6394a90ae4da
SPL ID
211625cc-0d51-9f5d-e063-6294a90a9341
Version
2
Effective date
2024-09-01
Source export date
2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:12:52

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 When using this product avoid unnecessary sun exposure and use a sunscreen. Keep away from eyes, lips, and mouth. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occcurs, only one medication should be used unless directed by a doctor. Avoid contact with hair and dyed fabrics, which may be bleached by this product.

Reported adverse events (FAERS/openFDA)#

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