FDA label 7d8a2e59-5602-488a-9775-8ff940cffc03

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
a06ed13a-2ecf-43b9-8599-4cdc2b707b0b
SPL ID
7d8a2e59-5602-488a-9775-8ff940cffc03
Version
1
Effective date
2016-12-15
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:43:35

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 are sensitive to benzoyl peroxide When using this product avoid unnecessary sun exposure and use a sunscreen if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor avoid contact with eyes, lips and mouth avoid contact with hair or dyed fabrics, including carpet and clothing which may be bleached by this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time 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. Stop use and ask a doctor if skin irritation or redness becomes severe. Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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