FDA label 5d8a1af9-0bbd-45cd-8fde-0eac5602ae2b

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
8ab7489d-97cf-4323-8e27-dc668ae823eb
SPL ID
5d8a1af9-0bbd-45cd-8fde-0eac5602ae2b
Version
7
Effective date
2011-08-16
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:11:29

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

Warning: For external use only. When using other topical acne drugs at the same time or right after use of this product may increase dryness, redness or irritation of the skin. If this occurs, only one product should be used unless directed by a health care practitioner. When using this product: avoid contact with eyes, lips, mouth and nostrils; if contact occurs rinse thoroughly with water. Stop use if excessive skin irritation develops or increases. If irritation persists, consult a health care practitioner. This product may bleach hair or dyed fabrics. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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