FDA.reportPublic FDA data

Acne Control Serum

Manufacturer
Private Label Skin Care
Effective date
2026-06-03
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-05 00:30:43

Label at a glance#

ProductAcne Control Serum
Active ingredientBENZOYL PEROXIDE
Label structure8 sections

Indications and uses

• for the treatment of acne • helps prevent new acne blemishes from forming

Dosage and administration

• wash the skin thoroughly before applying this product • Apply affected area with a thin layer, avoiding eye area • Allow to absorb before applying additional products. • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two times daily if needed or as directed by a doctor • if bothersome dryness or peeling occurs, reduce application to once a day or ever...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide 5%

Purpose

OTC - PURPOSE SECTION

Acne Medication

Uses

INDICATIONS & USAGE SECTION

• for the treatment of acne • helps prevent new acne blemishes from forming

Warnings

WARNINGS SECTION

For external use only

Do not use if you • have very sensitive skin • are sensitive to benzoyl peroxide

When using this product • 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 a lower concentration • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a 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

Stop use and ask a doctor if • irritation becomes severe

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wash the skin thoroughly before applying this product • Apply affected area with a thin layer, avoiding eye area • Allow to absorb before applying additional products. • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two times daily if needed or as directed by a doctor • if bothersome dryness or peeling occurs, reduce application to once a day or every other day • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Glycolic Acid, Sclerotium Gum, Arnica (Arnica Montana) Flower Extract, Calendula (Calendula Officinalis) Flower Extract, ConeFlower (Echinacea Purpurea) Extract, Goldenseal (Hydrastis Canadensis) Extract, Lavender (Lavandula Angustifolia) Flower Extract, Gluconolactone, Sodium Hydroxide, Sodium Benzoate, Allantoin, Tetrasodium EDTA, Glycerin

SPL UNCLASSIFIED SECTION

brand MD

Benzoyl Peroxide 5% Acne Treatment

Glycolic Acid 5%
Calendula
Arnica

MEDICAL GRADE

CLEAR

RECOMMENDED FOR
• BLEMISH- PRONE
• COMBO  • OILY

GREEN LEAF PROGRAM

NOT TESTED ON ANIMALS

Distributed by:
brandMD®
Canoga Park, CA 91304
(818) 534-3180
www.brandMD.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

acne controlacne control

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

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72957-00172957-001-01
39765-030

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOYL PEROXIDEW9WZN9A0GMACTIB
WATER059QF0KO0RIACT
GLYCOLIC ACID0WT12SX38SIACT
BETASIZOFIRAN2X51AD1X3TIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
ECHINACEA PURPUREA WHOLEQI7G114Y98IACT
GOLDENSEALZW3Z11D0JVIACT
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER19AH1RAF4MIACT
GLUCONOLACTONEWQ29KQ9POTIACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM BENZOATEOJ245FE5EUIACT
ALLANTOIN344S277G0ZIACT
EDETATE SODIUMMP1J8420LUIACT
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-02-26full-release2026-06-01 00:57:13

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
Acne Control SerumBENZOYL PEROXIDEPrivate Label Skin Cared4a4b89f-c9cf-4188-9c61-e8ef22b7638c2026-06-03WarningsExact identifier
ndc (package): 72957-001-01
ndc (product): 72957-001
ndc11 (package): 72957000101
spl id: 9baed740-4c05-4d87-9af7-997e36a98850
spl set id: d4a4b89f-c9cf-4188-9c61-e8ef22b7638c

Reported adverse events (FAERS/openFDA)#

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