NEUTROGENA RAPID CLEAR FOAMING SCRUB- salicylic acid lotion 
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.

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Neutrogena® Rapid Clear® Foaming Scrub

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne treatment

Use

For the treatment of acne.

Warnings

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.
  • avoid contact with eyes. If 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.

Directions

  • Cleanse twice a day. Wet face. Apply to hands, add water and work into a lather.
  • Massage gently.
  • Rinse thoroughly.

Other information

Store at Room Temperature

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Polyethylene, Acrylates Copolymer, Sodium Chloride, Fragrance, Polysorbate 20, Sodium Hydroxide, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Polyquaternium-7, Menthol, Cocamidopropyl PG-Dimonium Chloride Phosphate, Sodium Benzotriazolyl Butylphenol Sulfonate, Carrageenan, Agar, Ascorbyl Palmitate, Butylene Glycol, Propylene Glycol, Camellia Oleifera Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid, Iron Oxides, Yellow 5, Red 40, Mica, Red 30, Titanium Dioxide

Questions?

Call toll-free 800-582-4048 or 215-273-8755 (collect). www.neutrogena.com

Dist. by Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label

NEW INFO
NEUTROGENA
Rapid
Clear®
Foaming Scrub

MICROCLEAR®
technology

visibly reduces
breakouts

Neutrogena®

salicylic acid acne treatment
4.2 FL OZ (125mL)

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label
NEUTROGENA RAPID CLEAR FOAMING SCRUB 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-328
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)  
Glycerin (UNII: PDC6A3C0OX)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
High Density Polyethylene (UNII: UG00KM4WR7)  
Sodium Chloride (UNII: 451W47IQ8X)  
Polysorbate 20 (UNII: 7T1F30V5YH)  
Sodium Hydroxide (UNII: 55X04QC32I)  
C12-15 Alkyl Lactate (UNII: GC844VRD7E)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Edetate Disodium (UNII: 7FLD91C86K)  
Menthol, Unspecified Form (UNII: L7T10EIP3A)  
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
Sodium Benzotriazolyl Butylphenol Sulfonate (UNII: 0LA2QC9O3Z)  
Carrageenan (UNII: 5C69YCD2YJ)  
AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)  
Ascorbyl Palmitate (UNII: QN83US2B0N)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Camellia Oleifera Leaf (UNII: 5077EL0C60)  
Chamomile (UNII: FGL3685T2X)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Ferric Oxide Red (UNII: 1K09F3G675)  
Fd&C Yellow No. 5 (UNII: I753WB2F1M)  
Fd&C Red No. 40 (UNII: WZB9127XOA)  
Mica (UNII: V8A1AW0880)  
D&C Red No. 30 (UNII: 2S42T2808B)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-328-01125 mL in 1 TUBE; Type 0: Not a Combination Product06/01/201010/13/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D06/01/201010/13/2016
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 10/2016
Document Id: ab3ab2e8-04b8-4544-be23-f1106ade0fdd
Set id: d72a6343-0d74-4a52-84d8-f7f8ece6d682
Version: 3
Effective Time: 20161017
 
Johnson & Johnson Consumer Inc.