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Neutrogena Blackhead Eliminating Daily Scrub

Dosage form: gel
Ingredients: Salicylic Acid 20mg in 1mL
Labeler: Johnson & Johnson Consumer Inc.
NDC Code: 69968-0137

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.

Neutrogena® Blackhead Eliminating 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, cellulose, PPG-15 stearyl ether, glycerin, polysorbate 60, steareth-21, potassium cetyl phosphate, xanthan gum, fragrance, disodium EDTA, menthyl lactate, sodium hydroxide, agar, iron oxides, mica, titanium dioxide, red 30

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

NEW &
IMPROVED

Blackhead
Eliminating
DAILY
SCRUB

  • penetrates to eliminate
    most blackheads and
    helps prevent new ones
  • gently exfoliates

Neutrogena®

salicylic acid acne treatment

4.2 FL. OZ. (124mL)

NEUTROGENA BLACKHEAD ELIMINATING DAILY SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0137
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (Salicylic Acid) Salicylic Acid20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Cetyl Alcohol 
PPG-15 Stearyl Ether 
Powdered Cellulose 
Glycerin 
Steareth-21 
Polysorbate 60 
Potassium Cetyl Phosphate 
Xanthan Gum 
Sodium Hydroxide 
Edetate Disodium 
AGAR, UNSPECIFIED 
Menthyl Lactate, (-)- 
Ferric Oxide Red 
Mica 
Titanium Dioxide 
D&C Red No. 30 
Packaging
#Item CodePackage Description
1NDC:69968-0137-1124 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D06/01/2016
Labeler - Johnson & Johnson Consumer Inc. (002347102)

 
Johnson & Johnson Consumer Inc.

Medically reviewed on Nov 17, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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