FDA label ebf7b326-0f29-5d06-e053-2a95a90aea77

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
d00e93b6-8af5-4597-ac14-de2b7663b828
SPL ID
ebf7b326-0f29-5d06-e053-2a95a90aea77
Version
14
Effective date
2022-10-31
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:28

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. When using this product skin irritation and dryness is more likel to occur if you use another topical acne medication at the same time. Avoid unnecessary sun exposure and use a sunscreen. Avoid Contact with the eyes, lips and mouth. Avoid contact with hair and dyed fabrics, which may be bleached by this product. Skin irritation may occur and may be reduced by using the product less requently. Do not use if you have very sensitive skin, or are sensitive to Benzoyl Peroxide. 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.