Neutrogena ® Rapid Clear ® Foaming Scrub

Neutrogena Rapid Clear Foaming Scrub by

Drug Labeling and Warnings

Neutrogena Rapid Clear Foaming Scrub by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEUTROGENA RAPID CLEAR FOAMING SCRUB- salicylic acid gel 
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, Microcrystalline Cellulose, Sodium Chloride, Acrylates Copolymer, Fragrance, Polysorbate 20, Sodium Hydroxide, Disodium EDTA, C12-15 Alkyl Lactate, Benzalkonium Chloride, Polyquaternium-7, Menthol, Cocamidopropyl PG-Dimonium Chloride Phosphate, Sodium Benzotriazolyl Butylphenol Sulfonate, Carrageenan, Agar, Ascorbyl Palmitate, Iron Oxide, Yellow 5, Red 40, Mica, Red 30, Titanium Dioxide

Questions?

Call toll-free 800-299-4786 or 215-273-8755 (collect). www.neutrogena.com

Distributed By:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label

NEUTROGENA

Rapid
Clear ®

Foaming Scrub

MICROCLEAR ®
technology

visibly reduces
breakouts

Neutrogena ®

salicylic acid acne treatment

4 FL. OZ. (125 mL)

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label
NEUTROGENA RAPID CLEAR FOAMING SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69968-0695
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)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
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)  
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: 69968-0695-4125 mL in 1 TUBE; Type 0: Not a Combination Product09/28/202001/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D09/28/202001/02/2022
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 6/2021