NEUTROGENA BLACKHEAD ELIMINATING DAILY SCRUB- salicylic acid gel

Neutrogena Blackhead Eliminating Daily Scrub by

Drug Labeling and Warnings

Neutrogena Blackhead Eliminating Daily Scrub by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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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

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

PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

Blackhead
Eliminating
daily scrub

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

salicylic acid acne treatment
4.2 FL. OZ. (124mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA BLACKHEAD ELIMINATING DAILY SCRUB 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cetyl Alcohol (UNII: 936JST6JCN)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
PPG-15 Stearyl Ether (UNII: 1II18XLS1L)
Glycerin (UNII: PDC6A3C0OX)
Polysorbate 60 (UNII: CAL22UVI4M)
Steareth-21 (UNII: 53J3F32P58)
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)
Xanthan Gum (UNII: TTV12P4NEE)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
Sodium Hydroxide (UNII: 55X04QC32I)
AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)
FERRIC OXIDE RED (UNII: 1K09F3G675)
Mica (UNII: V8A1AW0880)
Titanium Dioxide (UNII: 15FIX9V2JP)
D&C RED NO. 30 (UNII: 2S42T2808B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0025-4	124 mL in 1 TUBE; Type 0: Not a Combination Product	06/17/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	06/17/2019

Labeler - Johnson & Johnson Consumer Inc. (002347102)