BENZOYL PEROXIDE 5% Topical wash

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)

Brand name: BENZOYL PEROXIDE 5% Topical wash
Generic name: BENZOYL PEROXIDE
Manufacturer: Medcore LLC
Product type: HUMAN OTC DRUG
SPL set ID: 14bf3034-2fe8-44b9-9e26-e804b6046837
SPL ID: 14cd67f2-dc7d-484b-bd21-bcb09c7f779e
Version: 1
Effective date: 2025-10-22
Source export date: 2026-10-27
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:08:49

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M006	openfda.application_number
brand name		BENZOYL PEROXIDE 10% Topical wash	openfda.brand_name
brand name		BENZOYL PEROXIDE 5% Topical wash	openfda.brand_name
generic name		BENZOYL PEROXIDE	openfda.generic_name
manufacturer name		Medcore LLC	openfda.manufacturer_name
ndc	package	82461-313-05	openfda.package_ndc
ndc	package	82461-312-05	openfda.package_ndc
ndc	package	82461-313-08	openfda.package_ndc
ndc	package	82461-312-08	openfda.package_ndc
ndc	product	82461-312	openfda.product_ndc
ndc	product	82461-313	openfda.product_ndc
ndc11	package	82461031208	derived:openfda.package_ndc
ndc11	package	82461031308	derived:openfda.package_ndc
ndc11	package	82461031305	derived:openfda.package_ndc
ndc11	package	82461031205	derived:openfda.package_ndc
rxcui		142034	openfda.rxcui
rxcui		308696	openfda.rxcui
spl id		14cd67f2-dc7d-484b-bd21-bcb09c7f779e	id
spl set id		14bf3034-2fe8-44b9-9e26-e804b6046837	set_id
unii		W9WZN9A0GM	openfda.unii

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. Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. Avoid unnessary sun exposure and use a sunscreen. Avoid contact with eyes, lips and mouth. Avoid contact with hair,dyed fabrics, which may be bleached by thisproduct. 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 lower concentration.If irritation or sensitivy develops stop use of both products and ask a doctor.

Reported adverse events (FAERS/openFDA)#

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