NEUTROGENA BODY CLEAR BODY SCRUB- salicylic acid suspension

Neutrogena Body Clear Body Scrub by

Drug Labeling and Warnings

Neutrogena Body Clear Body 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

Use daily in the shower or bath.

• For maximum lather, massage over wet skin with a washcloth or body puff, concentrating on areas prone to breakouts.
• Rinse well.

Other information

Store at Room Temperature.

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Microcrystalline Cellulose, Sodium Chloride, Acrylates Copolymer, Cellulose, Fragrance, Sodium Hydroxide, Disodium EDTA, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Yellow 6, Yellow 5, Red 40, Red 33, Blue 1

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 - 250 mL Bottle Label

Body
Clear®
Body Scrub

treats and helps prevent
body breakouts for
smooth, clear skin

with aloe and chamomile

salicylic acid acne treatment

Neutrogena®
DERMATOLOGIST RECOMMENDED

8.5 FL. OZ. (250 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA BODY CLEAR BODY SCRUB 
salicylic acid suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0628
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)
Sodium Chloride (UNII: 451W47IQ8X)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
Sodium Hydroxide (UNII: 55X04QC32I)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMOMILE (UNII: FGL3685T2X)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0628-9	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	02/24/2020

Labeler - Johnson & Johnson Consumer Inc. (002347102)