NEUTROGENA ACNE PROOFING DAILY SCRUB- salicylic acid gel

Neutrogena Acne Proofing daily scrub by

Drug Labeling and Warnings

Neutrogena Acne Proofing 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]

SPL UNCLASSIFIED SECTION

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 Rome Temperature

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol Cellulose, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Acrylates Crosspolymer-4, Panthenol, Sodium Hydroxide, Fragrance, Microcrystalline Wax, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Cocamidopropyl PG-Dimonium Chloride Phosphate, Talc, Yellow 5 Lake, Red 30

Questions?

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 119 g Tube Label

NEW

Acne
Proofing™
daily scrub
clears breakouts and helps
defend against new ones to make
skin more acne resistant

CLEARDEFEND
TECHNOLOGY ™

maximum strength
salicylic acid acne treatment

Neutrogena®
DERMATOLOGIST RECOMMENDED
NET WT . 4.2 OZ. (119 g)

INGREDIENTS AND APPEARANCE

NEUTROGENA ACNE PROOFING DAILY SCRUB 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0112
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 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
Sorbitol (UNII: 506T60A25R)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
Panthenol (UNII: WV9CM0O67Z)
Sodium Hydroxide (UNII: 55X04QC32I)
Microcrystalline Wax (UNII: XOF597Q3KY)
C12-15 Alkyl Lactate (UNII: GC844VRD7E)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
D&C RED NO. 30 (UNII: 2S42T2808B)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
Talc (UNII: 7SEV7J4R1U)
FD&C Yellow No. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0112-4	119 g in 1 TUBE; Type 0: Not a Combination Product	10/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	10/01/2017

Labeler - Johnson & Johnson Consumer Inc. (002347102)