2.5 ACNE MED- benzoyl peroxide gel 
Face Reality, Inc.

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2.5 % Acne Med

Drug Facts

Active ingredient

Benzoyl Peroxide 2.5%

Purpose

Acne Treatment

Use

Warnings

For external use only

Do not use

  • if you have very sensitive skin
  • if you are sensitive to benzoyl peroxide

When using this product

  • 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 eyes, lips and mouth
  • avoid contact with hair and dyed fabrics, 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.

Stop use and ask a doctor if

  • irritation becomes severe

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

Purified Water, Glycerin, Propylene Glycol, Carbomer, Sodium Hydroxide.

Questions or Comments?

1-866-477-3077

Package Labeling:

Bottle2Tube

2.5 ACNE MED 
benzoyl peroxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70707-152
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70707-152-151 in 1 CARTON11/23/2011
144 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00611/23/2011
Labeler - Face Reality, Inc. (602958071)

Revised: 10/2023
Document Id: 08a1e862-b55e-fb84-e063-6294a90a016a
Set id: 58a7f677-996c-4951-8e5d-b5556244f800
Version: 2
Effective Time: 20231026
 
Face Reality, Inc.