ACNE CONTROL SERUM- benzoyl peroxide lotion 
Private Label Skin Care

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Acne Control Serum

Drug Facts

Active ingredient

Benzoyl Peroxide 5%

Purpose

Acne Medication

Use For the treatment of acne.

Warnings For external use only.

When using this product • avoid unnecessary sun exposure and use sunscreen. • avoid contact with eyes, lips and mouth. • avoid contact with hair and dyed products, which may be bleached by 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

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

Directions • Clean the skin thoroughly before applying this product. Apply affected area with a thin layer, avoiding eye area. Allow to absorb before applying additional products. Can be used twice daily or as directed by physician. If irritation or sensitivity develops, stop use of product and consult physician.

Inactive Ingredients Deionized Water, Glycolic Acid, Sclerotium Gum, Arnica Montana Flower Extract, Allantoin, Echinacea Purpurea Extract, Hydrastis Canadensis (Golden seal) Extract, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Calendula Officinalis Flower Extract, Glycerin, Gluconolactone, Sodium Benzoate, Tetrasodium EDTA, Sodium Hydroxide

brand MD®

SKIN CARE

ACNE DEFENSE

medical grade

Clinically proven to decrease sebum production by up to 70%

Fights acne-causing bacteria on the spot and prevents future breakouts

brandMD® Chatsworth, CA 91311

www.brandMD.com

Made in USA

Packaging

Acne1

ACNE CONTROL SERUM 
benzoyl peroxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72957-001(NDC:39765-030)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
BETASIZOFIRAN (UNII: 2X51AD1X3T)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
ALLANTOIN (UNII: 344S277G0Z)  
ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98)  
GOLDENSEAL (UNII: ZW3Z11D0JV)  
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72957-001-0132 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/23/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D01/23/2020
Labeler - Private Label Skin Care (116996962)
Establishment
NameAddressID/FEIBusiness Operations
Private Label Skin Care116996962relabel(72957-001)

Revised: 1/2022
Document Id: 28ef1bb5-0d0c-4a3f-8ccd-636e86ad362e
Set id: d4a4b89f-c9cf-4188-9c61-e8ef22b7638c
Version: 3
Effective Time: 20220120
 
Private Label Skin Care