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Neutrogena SkinClearing Mineral - Honey Beige

Dosage form: powder
Ingredients: Salicylic Acid 5mg in 1g
Labeler: Johnson & Johnson Consumer Inc.
NDC Code: 10812-513

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® SkinClearing® Mineral Powder

Drug Facts

Active ingredient

Salicylic Acid 0.5%


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.
  • if eye contact occurs, flush thoroughly with water.

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

  • cleanse skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other information

Protect from Excessive Heat (40°C/104°F).

Inactive ingredients

Talc, Dimethicone, Zinc Stearate, Polyethylene, Octyldodecyl Stearoyl Stearate, Mica, C12-15 Alkyl Benzoate, Nylon-12, Polysilicone-11, Petrolatum, Ethylene/Acrylic Acid Copolymer, Calcium Silicate, Sodium Dehydroacetate, Methylparaben, Retinyl Palmitate, Tocopheryl Acetate, Propylparaben, Panthenol, Polymethyl Methacrylate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cetyl Lactate, C12-15 Alkyl Lactate, Benzalkonium Chloride, Ascorbyl Palmitate, Tocoheryl Acetate, Pantothenic Acid, Ascorbic Acid.

May Contain: Titanium Dioxide, Iron Oxides, Carmine, Zinc Oxide.


Call toll-free 800-480-4812 or 215-273-8755 (collect) or

Dist. by Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 11 g Container Label


- technology -

salicylic acid powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-513
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (Salicylic Acid) Salicylic Acid5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Zinc Stearate 
High Density Polyethylene 
Octyldodecyl Stearoyl Stearate 
Alkyl (C12-15) Benzoate 
Calcium Silicate 
Sodium Dehydroacetate 
Vitamin A Palmitate 
.Alpha.-Tocopherol Acetate 
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate 
Cetyl Lactate 
C12-15 Alkyl Lactate 
Benzalkonium Chloride 
Ascorbyl Palmitate 
Pantothenic Acid 
Ascorbic Acid 
Titanium Dioxide 
Ferric Oxide Red 
Zinc Oxide 
#Item CodePackage Description
1NDC:10812-513-1111 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D11/30/200912/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2016
Johnson & Johnson Consumer Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.