NEUTROGENA ALL IN 1 ACNE CONTROL  DAILY SCRUB- salicylic acid liquid 
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® All-in-1 Acne Control Daily 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 face gently.
  • Rinse thoroughly.

Other information

Store at Room Temperature.

Inactive ingredients

Water, Cetyl Alcohol, PPG-15 Stearyl Ether, Polyethylene, Steareth-21, Polysorbate 60, Potassium Cetyl Phosphate, Xanthan Gum, Fragrance, Disodium EDTA, Menthyl Lactate, Sodium Hydroxide, Glycine Soja (Soybean) Seed Extract

Questions?

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

Dist. by Neutrogena Corp.,
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label

NEW INFO

All-in-1
Acne
Control
daily scrub

clears up acne's
past, present & future

  • fades the look of past acne marks
  • clears present breakouts
  • helps prevent future breakouts

Neutrogena®

salicylic acid acne treatment

4.2 FL. OZ. (125mL)

Principal Display Panel - 125 mL Tube Label
NEUTROGENA ALL IN 1 ACNE CONTROL   DAILY SCRUB
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-398
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)  
Cetyl Alcohol (UNII: 936JST6JCN)  
High Density Polyethylene (UNII: UG00KM4WR7)  
Steareth-21 (UNII: 53J3F32P58)  
Polysorbate 60 (UNII: CAL22UVI4M)  
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)  
Xanthan Gum (UNII: TTV12P4NEE)  
Edetate Disodium (UNII: 7FLD91C86K)  
Menthyl Lactate, (-)- (UNII: 2BF9E65L7I)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Soybean (UNII: L7HT8F1ZOD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-398-01125 mL in 1 TUBE; Type 0: Not a Combination Product11/30/201106/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D11/30/201106/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 6/2016
Document Id: fea37ec8-de21-4c0e-9e3a-c8d6c1fe735d
Set id: 094c736e-4d58-4cac-9edc-c978d52bc0a3
Version: 3
Effective Time: 20160601
 
Johnson & Johnson Consumer Inc.