NEUTROGENA RAPID CLEAR FOAMING SCRUB- salicylic acid gel

Neutrogena Rapid Clear Foaming Scrub by

Drug Labeling and Warnings

Neutrogena Rapid Clear Foaming 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 gently.
• Rinse thoroughly.

Other Information

Store at Room Temperature.

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Microcrystalline Cellulose, Acrylates Copolymer, Fragrance, Polysorbate 20, Sodium Hydroxide, C12-15 Alkyl Lactate, Benzalkonium Chloride, Polyquaternium-7, Disodium EDTA, Menthol, Cocamidopropyl PG-Dimonium Chloride Phosphate, Sodium Benzotriazolyl Butylphenol Sulfonate, Carrageenan, Agar, Ascorbyl Palmitate, Iron Oxides, Yellow 5, Red 40, Mica, Red 30, Titanium Dioxide

Questions?

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label

NEW &
IMPROVED
NEUTROGENA
Rapid
Clear®
Foaming Scrub

MICROCLEAR®
technology

visibly reduces
breakouts

Neutrogena®

salicylic acid acne treatment
4.2 FL OZ (125mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA RAPID CLEAR FOAMING SCRUB 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0128
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)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Glycerin (UNII: PDC6A3C0OX)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Microcrystalline Cellulose (UNII: OP1R32D61U)
Polysorbate 20 (UNII: 7T1F30V5YH)
Sodium Hydroxide (UNII: 55X04QC32I)
C12-15 Alkyl Lactate (UNII: GC844VRD7E)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)
Polyquaternium-7 (70/30 Acrylamide/Dadmac; 1600000 Mw) (UNII: 0L414VCS5Y)
Menthol, Unspecified Form (UNII: L7T10EIP3A)
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)
Sodium Benzotriazolyl Butylphenol Sulfonate (UNII: 0LA2QC9O3Z)
Carrageenan (UNII: 5C69YCD2YJ)
Agar, Unspecified (UNII: 89T13OHQ2B)
Ascorbyl Palmitate (UNII: QN83US2B0N)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Ferric Oxide Red (UNII: 1K09F3G675)
Fd&C Yellow No. 5 (UNII: I753WB2F1M)
Fd&C Red No. 40 (UNII: WZB9127XOA)
Mica (UNII: V8A1AW0880)
D&C Red No. 30 (UNII: 2S42T2808B)
Titanium Dioxide (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0128-4	125 mL in 1 TUBE; Type 0: Not a Combination Product	10/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	10/01/2016

Labeler - Johnson & Johnson Consumer Inc. (002347102)