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Acne Control Serum

Dosage form: gel
Ingredients: BENZOYL PEROXIDE 5mL in 100mL
Labeler: Neutraderm, Inc.
NDC Code: 39765-005

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.

Drug Facts

Active Ingredient

Benzoyl peroxide 5%

Purpose

Acne Treatment

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away.

Directions

Apply over face and neck avoiding eye area. Allow to absorb before applying additional products. Can be used twice daily or as directed by Physician.

Warning

For external use only

Dosage

Use twice daily or as directed by Physician.

Inactive Ingredients

Deionized Water, Glycolic Acid, Sclerotium Gum, Amica Montana Flower Extract, Allantoin, Echinacea Purpurea Extract, Hydrastis Canadensis (Golden Seal) Extract, Lavandula Angustifolia (Lanvender) Flower/Leaf Stem Extract, Calendula Officinalis Flower Extract, Glycerin, Gluconolactone, Sodium Benzoate, Tetrasodium EDTA, Sodium Hydroxide.

Product Label

ACNE CONTROL SERUM  
benzoyl peroxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39765-005
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE) BENZOYL PEROXIDE5 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCOLIC ACID 
BETASIZOFIRAN 
ARNICA MONTANA FLOWER 
ALLANTOIN 
ECHINACEA PURPUREA 
GOLDENSEAL 
LAVANDULA ANGUSTIFOLIA FLOWERING TOP 
CALENDULA OFFICINALIS FLOWER 
GLYCERIN 
GLUCONOLACTONE 
SODIUM BENZOATE 
EDETATE SODIUM 
SODIUM HYDROXIDE 
Product Characteristics
Colorwhite (Off-White) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:39765-005-0130 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D07/01/2010
Labeler - Neutraderm, Inc. (146224444)
Establishment
NameAddressID/FEIOperations
Neutraderm, Inc.146224444manufacture(39765-005)

 
Neutraderm, Inc.

Medically reviewed on Aug 6, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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