NEUTROGENA ALL IN 1 ACNE CONTROL DAILY SCRUB- salicylic acid liquid

Neutrogena All in 1 Acne Control Daily Scrub by

Drug Labeling and Warnings

Neutrogena All in 1 Acne Control 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, PPG-15 stearyl ether, cellulose, glycerin, Polysorbate 60, steareth-21, potassium cetyl phosphate, xanthan gum, fragrance, disodium EDTA, menthyl lactate, sodium hydroxide

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

NEW &
IMPROVED

All-in-1
Acne
Control
daily scrub

works on acne's
past, present & future

• exfoliates past acne marks
• clears present breakouts
• helps prevent future breakouts

Neutrogena®

salicylic acid acne treatment

4.2 FL. OZ. (124mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA ALL IN 1 ACNE CONTROL DAILY SCRUB 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0092
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)
PPG-15 Stearyl Ether (UNII: 1II18XLS1L)
Powdered Cellulose (UNII: SMD1X3XO9M)
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)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0092-4	124 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	06/01/2016

Labeler - Johnson & Johnson Consumer Inc. (002347102)