FDA label e6fcc8a4-dc13-4810-9d80-fcf64e418473

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
0b54b656-ca74-47da-8a49-119a0cb48b26
SPL ID
e6fcc8a4-dc13-4810-9d80-fcf64e418473
Version
2
Effective date
2015-11-23
Source export date
2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:01

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 Stop use and ask a Doctor if too much skin irritation or sensitivity develops or increases Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use if you have very sensative skin are sensative to benzoyl peroxide have broken skin When using this product, Avoid unnecessary sun exposure and use a sunscreen. Avoid contact with the eyes, lips, and mouth. This product may bleach hair or dyed products. Using other topical acne drugs at the same time or right after use of this product may increase dryness or irriatation of the skin.

Reported adverse events (FAERS/openFDA)#

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