FDA.reportPublic FDA data

Benzoyl Peroxide

Manufacturer
Malezia LLC
Effective date
2026-08-11
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
daily-update
Hydrated at
2026-08-14 00:01:11

Label at a glance#

ProductBenzoyl Peroxide
Active ingredientBENZOYL PEROXIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 mL NDC: 77924-002-01

Front of Malezia BP LabelFront of Malezia BP Label

Back of BP LabelBack of BP Label

DOSAGE & ADMINISTRATION SECTION

50 mL NDC: 77924-002-01

dosage and adminstrationdosage and adminstration

WARNINGS SECTION

50 mL NDC: 77924-002-01

Warning sectionWarning section

INACTIVE INGREDIENT SECTION

50 mL NDC: 77924-002-01

inactive ingredientsinactive ingredients

OTC - ACTIVE INGREDIENT SECTION

50 mL NDC: 77924-002-01

active ingredientactive ingredient

OTC - PURPOSE SECTION

50 mL NDC: 77924-002-01

purposepurpose

INDICATIONS & USAGE SECTION

50 mL NDC: 77924-002-01

indications and usageindications and usage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

50 mL NDC: 77924-002-01

children warningchildren warning

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a46239a7-5963-4008-8cbb-6b9000f497ebProduct name120250721
b382b4e1-6b48-45f6-bffc-e61b00b0ce19Product name320250317
d9d61457-6a5a-41fc-b418-e5479a2904b7Product name220230303
32012d5c-25ac-49c7-9d4c-1313177fff7cProduct name120230112
13e7e7e3-e885-4c79-af6d-dad1aedbb06eProduct name120220128
4a7d44fe-774d-404b-aad0-8a90fe78375aProduct name420211025
3f45980c-c196-47e5-0e5e-48b7c57327c5Product name520200428
d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27bProduct name320200203
ee5c6de5-d9cd-454f-b250-7b19e5cf2992Product name420190619
ad75fcfd-a339-42a1-9c60-43ba2c654cfaProduct name120170810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77924-002-022025-07-29C16284748780-11030e364-fb7c-111a-e063-dadaa90a10e2Benzoyl Peroxide
77924-002-022025-07-29C16284748780-11030e364-fb7c-111a-e063-dadaa90a10e2Benzoyl Peroxide
77924-002-022024-01-31C16284748780-11030e364-fb7c-111a-e063-dadaa90a10e2Benzoyl Peroxide
77924-002-022024-01-31C16284748780-11030e364-fb7c-111a-e063-dadaa90a10e2Benzoyl Peroxide

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77924-00277924-002-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOYL PEROXIDEW9WZN9A0GMACTIB
GLYCERINPDC6A3C0OXIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
CARBOMER 9804Q93RCW27EIACT
PHYTATE SODIUM88496G1ERLIACT
PROPANEDIOL5965N8W85TIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82024-10-30full-release2026-06-01 00:34:32

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Benzoyl PeroxideBENZOYL PEROXIDEMalezia LLCb1304464-bd7e-fb5d-e053-2995a90a54c42026-08-11WarningsExact identifier
ndc (package): 77924-002-02
ndc (product): 77924-002
ndc11 (package): 77924000202
spl id: 58ce7eef-7f98-0c96-e063-6394a90a8d2d
spl set id: b1304464-bd7e-fb5d-e053-2995a90a54c4

Reported adverse events (FAERS/openFDA)#

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