ACNE WIPEOUT ALL DAY BREAKOUT CONTROL- benzoyl peroxide cream 
University Medical Pharmaceuticals Corp.

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 WIPEOUT™ ALL DAY BREAKOUT CONTROL

Drug Facts

Active ingredient

Benzoyl Peroxide 5% w/v

Purpose

Acne treatment

Use

• For the treatment of acne

Warnings

For external use only.

Do not use • If you are sensitive to Benzoyl Peroxide or have very sensitive skin. This product may cause irritation. Ask a doctor or pharmacist before use • If you are using other topical acne drugs at the same time or right after use of this product. This may increase dryness, redness or irritation of the skin. If this occurs, only one medication should be used unless a doctor directs otherwise.
When using this product • Avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep away from lips and mouth. • Avoid unnecessary sun exposure and use a sunscreen. • Avoid product contact with hair and dyed fabrics, including towels, carpets and clothing which may be bleached by this product.

Stop use and ask a doctor if
• excessive irritation occurs.

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

Directions

Adults and children 12 years of age and older:
Use every morning after cleansing with Acne Wipeout™ Clear Pore Oil-Free Cleanser. Apply a dime-size amount to clean skin, avoiding the eye area. Do not rinse. If bothersome dryness or irritation occurs, reduce frequency of use. May be applied all over face to help control future breakouts.

Other information

Inactive Ingredients

Water (Aqua), Sodium C14-16 Olefin Sulfonate, PEG-8, Disodium Laureth Sulfosuccinate, Polyacrylate-1 Crosspolymer, Cocamidopropyl Betaine, Allyl Methacrylates Crosspolymer, Butylene Glycol, Glycerin, DMDM Hydantoin, Tocopheryl Acetate (Vitamin E Acetate), Glycyrrhiza Glabra (Licorice) Root Extract, Calendula Officinalis Flower Extract, Hamamelis Virginiana (Witch Hazel) Extract, Citric Acid, Tetrasodium EDTA, Sodium Hydroxide, Fragrance, Sodium Benzotriazolyl Butylphenol Sulfonate, Benzoic Acid.

Questions? call toll free 855-299-8800

DERMATOLOGICAL FIRST LINE ACNE CARE

HYDRATING CREAM

TIME-RELEASED

5% BENZOYL PEROXIDE ACNE TREATMENT

MINIMIZES IRRITATION AND DRYNESS

PART OF THE ACNE WIPEOUT CLINICAL ACNE SYSTEM

acnewipeout.com

made in usa

UNIVERSITY MEDICAL

PHARMACEUTICALS CORP

9671 Irvine Center Drive

Irvine, CA 92618 ©2020


EFFECTIVE CLEARING + HYDRATION ALL DAY LONG

NON-COMEDOGENIC

FRAGRANCE FREE

PARABEN FREE

All Day Breakout Control delivers micronized, time-released benzoyl peroxide into pores to kill acne bacteria all day long—while hydrating skin and minimizing irritation and dryness.

Packaging

Hydrate1

ACNE WIPEOUT ALL DAY BREAKOUT CONTROL 
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50544-152
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
ALLYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: B9J55EA6QX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GLYCERIN (UNII: PDC6A3C0OX)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50544-152-001 in 1 CARTON06/01/2020
160 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D06/01/2020
Labeler - University Medical Pharmaceuticals Corp. (809706252)

Revised: 10/2020
Document Id: 13c12c8d-c652-4690-875f-aa63b4c94d0c
Set id: 2b004dfa-2c72-40ec-9b06-60502b3b6ce9
Version: 1
Effective Time: 20201002
 
University Medical Pharmaceuticals Corp.