FDA label 4a74b611-6d04-4298-a1ae-22b047488f0f

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
9bd6a779-74fd-4c44-8166-99e96b3e4865
SPL ID
4a74b611-6d04-4298-a1ae-22b047488f0f
Version
2
Effective date
2010-09-17
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:01:56

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 For external use only When using this product Skin irritation and dryness is more likely tooccur if you use other topical acne medications at the same time. If irritation occurs, only use one topical medication at a time. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away. Sunburn Alert: Use only as directed. This product contains an alpha hydroxy acid that may increase your skin’s sensitivity to the sun and particularly the possibility of sunburn. Please limit sun exposure and apply a sunburn protectant while using this product and for a week afterwards.

Reported adverse events (FAERS/openFDA)#

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