NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT- 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® 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 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 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

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, Cyclopentasiloxane, C12-15 Alkyl Lactate, Alcohol, Laureth-7, Phenoxyethanol, Cetyl Lactate, PPG-2 Isoceteth-20 Acetate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Polysorbate 20, Phenethyl Dimethicone, Fragrance, Dehydroxanthan Gum, Propylene Glycol, Benzalkonium Chloride, Ammonium Hydroxide, Tetrasodium EDTA, Butylene Glycol, Capryloyl Glycine, Hexylene Glycol, Sarcosine, Cinnamomum Zeylanicum Bark Extract, Cedrus Atlantica Bark Extract, Portulaca Oleracea Extract

Questions?

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

Dist. by
Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton

NEW INFO
NEUTROGENA
Rapid
Clear®

Acne
Eliminating
Spot Gel

MICROCLEAR®
technology

visibly reduces
breakouts in
8 HOURS

Neutrogena®

salicylic acid acne treatment

0.5 FL. OZ. (15mL)

Principal Display Panel - 15 mL Tube Carton
NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-206
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)  
Alcohol (UNII: 3K9958V90M)  
Hamamelis Virginiana Top Water (UNII: NT00Y05A2V)  
Glycerin (UNII: PDC6A3C0OX)  
C13-14 Isoparaffin (UNII: E4F12ROE70)  
Cyclomethicone 5 (UNII: 0THT5PCI0R)  
C12-15 Alkyl Lactate (UNII: GC844VRD7E)  
Laureth-7 (UNII: Z95S6G8201)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Cetyl Lactate (UNII: A7EVH2RK4O)  
PPG-2 Isoceteth-20 Acetate (UNII: BI6C7YO419)  
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
Polysorbate 20 (UNII: 7T1F30V5YH)  
Dehydroxanthan Gum (UNII: 63ZP7I1BQO)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Ammonia (UNII: 5138Q19F1X)  
Edetate Sodium (UNII: MP1J8420LU)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Capryloyl Glycine (UNII: 8TY5YO42NJ)  
Hexylene Glycol (UNII: KEH0A3F75J)  
Sarcosine (UNII: Z711V88R5F)  
Cinnamon Bark Oil (UNII: XE54U569EC)  
Cedrus Atlantica Bark (UNII: ITP1Q41UPF)  
Purslane (UNII: M6S840WXG5)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-206-011 in 1 CARTON
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 FINALpart333D10/13/201112/01/2017
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2015
Document Id: 3d3dee77-753c-45ea-a6b4-2dc7686c2656
Set id: 38005d41-8ed7-4de5-afcb-cce1496c3811
Version: 4
Effective Time: 20151221
 
Johnson & Johnson Consumer Inc.