NEUTROGENA CLEAR PORE DAILY SCRUB- benzoyl peroxide cream 
Johnson & Johnson Consumer Inc.

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.


Neutrogena Clear Pore Daily Scrub

Drug Facts

Active ingredient

Benzoyl Peroxide 3.7%


Acne medication


For the treatment of acne


For external use only

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.

Do not use if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

When using this product

  • avoid unnecessary sun exposure and use sunscreen
  • avoid contact with the 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

Stop use and ask a doctor if

  • irritation becomes severe

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


Products, such as soaps and masks, may be applied removed and should include appropriate directions

  • 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

Water, Glycerin, Kaolin, Bentonite, Sodium Methyl Cocoyl Taurate, Titanium Dioxide, Polyethylene, Sodium Chloride, Xanthan Gum, Citric Acid, Sodium Citrate, Trideceth-9, Disodium EDTA, Fragrance, PEG-5 Ethylhexanoate, and Menthol

Questions or comments?

1-800-582-4048 (USA only)

  • Avoid storage at extreme temperatures (below 40°F and above 100°F).




Daily Scrub

Benzoyl peroxide formula
penetrates pores to kill
breakout-causing bacteria


benzoyl peroxide acne medication

4.2 FL OZ (125 mL)

Principal Display Panel – 125 mL Bottle Label
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-404
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzoyl Peroxide (UNII: W9WZN9A0GM) (Benzoyl Peroxide - UNII:W9WZN9A0GM) Benzoyl Peroxide37 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Kaolin (UNII: 24H4NWX5CO)  
Bentonite (UNII: A3N5ZCN45C)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
Sodium Chloride (UNII: 451W47IQ8X)  
Xanthan Gum (UNII: TTV12P4NEE)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Sodium Citrate (UNII: 1Q73Q2JULR)  
Edetate Disodium (UNII: 7FLD91C86K)  
Menthol, Unspecified Form (UNII: L7T10EIP3A)  
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-404-01125 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D12/01/201012/08/2017
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2015
Johnson & Johnson Consumer Inc.