NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT- salicylic acid gel 
Johnson & Johnson Consumer Inc.

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Neutrogena Rapid Clear Acne Eliminating Spot Gel

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne medication

Use

For the treatment of acne.

Warnings

For external use only.

Flammable

Keep away from fire or flame.

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 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.

Directions

Other information

Sunburn Alert

This product contains an alpha hydroxy acid (AHA) that may increase your skin’s sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterwards.

Store at Room Temperature.

Inactive ingredients

Water, Alcohol Denat., Hamamelis Virginiana (Witch Hazel) Water, Polyacrylamide, Glycerin, C13-14 Isoparaffin, C12-15 Alkyl Lactate, Alcohol, Phenoxyethanol, Cetyl Lactate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Laureth-7, Polysorbate 20, Sodium Hydroxide, Phenethyl Dimethicone, Xanthan Gum, Propylene Glycol, Benzalkonium Chloride, Tetrasodium EDTA, Butylene Glycol, Capryloyl Glycine, Sarcosine, Cinnamomum Zeylanicum Bark Extract, Cedrus Atlantica Bark Extract, Portulaca Oleracea Extract

Questions?

800-299-4786; Outside US, dial collect 215-273-8755 or www.neutrogena.com

Distributed by:

JOHNSON & JOHNSON

CONSUMER INC.


Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton

NEUTROGENA

Rapid

Clear ®

Acne

Eliminating

Spot Gel

MICROCLEAR®

technology

Neutrogena®

salicylic acid acne treatment

0.5 FL OZ (15mL)

Neutrogena_01

NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0825
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
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
SARCOSINE (UNII: Z711V88R5F)  
CINNAMON BARK OIL (UNII: XE54U569EC)  
CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)  
PURSLANE (UNII: M6S840WXG5)  
WATER (UNII: 059QF0KO0R)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
ALCOHOL (UNII: 3K9958V90M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CETYL LACTATE (UNII: A7EVH2RK4O)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
LAURETH-7 (UNII: Z95S6G8201)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
EDETATE SODIUM (UNII: MP1J8420LU)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0825-11 in 1 CARTON08/30/2023
115 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/30/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 9/2023
Document Id: 06804af5-1bbf-d012-e063-6294a90a41de
Set id: 06804b81-db22-12ec-e063-6294a90a28e1
Version: 1
Effective Time: 20230929
 
Johnson & Johnson Consumer Inc.