FDA label dd7684e4-66ce-42a2-9deb-b5990f96a414

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
b2d9b887-8e8e-4f12-a260-2f47e0f3870e
SPL ID
dd7684e4-66ce-42a2-9deb-b5990f96a414
Version
2
Effective date
2017-12-07
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 05:40:14

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 Do not use ▄ If you have very sensitive skin, or if your skin is sensitive to benzoyl peroxide In rare instances, may cause severe allergic reactions or irritations that can be potentially life threatening. Avoid using if you have had previous allergic or hypersensitivity reaction. Stop using if you develop hives or itching of the face or body and seek immediate medical attention if you develop throat tightness or swelling of the eyes, face, lips, or tongue, feel faint, or have difficulty breathing. Using other topical acne medications at the same time or immediately following us of this product may increase dryness or irritation of the skin. If this occurs only one medication should be used unless otherwise directed by a healthcare professional. When using this product ▄ Avoid contact with the eyes. If contact does occur, rinse thoroughly with water. Keep away from lips and mouth. ▄ Avoid unnecessary sun exposure during use, and use a sunscreen with least a SPF of 15.

Reported adverse events (FAERS/openFDA)#

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