FDA label 99515059-4a2e-4176-99c2-30827fdbde5d

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
addefc6f-3a0a-4470-a4e8-a9398d354005
SPL ID
99515059-4a2e-4176-99c2-30827fdbde5d
Version
5
Effective date
2025-02-25
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:44:30

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 ♦ if you are sensitive to benzoyl peroxide When using this product ♦ avoid unnecessary sun exposure and use a sunscreen ♦ avoid contact with eyes, lips and mouth ♦ avoid contact with hair and dyed fabrics, which may be bleached by this product ♦ skin irritation and dryness is more likely to occur if you use another acne medication at the same time. If irritation occurs, use only 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 this product less frequently or at a lower concentration Stop use and ask a doctor if ♦ irritation becomes severe Keep out of reach of children ♦ if swallowed, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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