FDA label 69cc0b73-7ad3-4a43-82c9-c0dced9b9e52

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
08b5b8b7-551c-4e9b-b5a7-4e92de627a8c
SPL ID
69cc0b73-7ad3-4a43-82c9-c0dced9b9e52
Version
20502
Effective date
2012-05-21
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:30

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. Avoid contact with eyes. Keep out of reach of children . If swallowed get medical help or contact a Poison Control Center right away. When using this product. If excessive skin irritation appears persists, discontinue use and consult your physician. Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If it occurs, only one drug should be used unless directed by a physician. Avoid contact with eyes.

Reported adverse events (FAERS/openFDA)#

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