FDA label 6f5ae68f-a214-4e08-99ee-4175eb0d6dcc

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
14c7add7-2ef7-4322-a1a4-97109ba4a2aa
SPL ID
6f5ae68f-a214-4e08-99ee-4175eb0d6dcc
Version
1
Effective date
2018-05-04
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:42:05

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. Do not use if you have very sensitive skin or if you are sensitive to benzoyl peroxide. Stop use and ask a doctor if irritation becomes severe. When using this product : ■ avoid unnecessary sun exposure and use a sunscreen ■ using other topical acne drugs at the same time or right after use may increase dryness or irritation of skin. If this occurs, only one drug should be used ■ skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration ■ keep away from eyes, lips and mouth ■ 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.