NEUTROGENA BODY CLEAR BODY WASH- salicylic acid solution

Neutrogena Body Clear Body Wash by

Drug Labeling and Warnings

Neutrogena Body Clear Body Wash 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

• 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, Cocamidopropyl Betaine, Disodium Cocoamphodiacetate, Sodium Chloride, Glycerin, Sodium Methyl Cocoyl Taurate, Propylene Glycol, Fragrance, Linoleamidopropyl PG-Dimonium Chloride Phosphate, Citric Acid, Chamomilla Recutita (Matricaria) Flower Extract, Anthemis Nobilis Flower Extract, Aloe Barbadensis Leaf Extract, Yellow 5, Red 33

Questions?

Call toll-free 866-638-4636 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 Wash

treats and helps prevent
body breakouts for
clean, clear skin

salicylic acid acne treatment

Neutrogena®
DERMATOLOGIST RECOMMENDED

8.5 FL. OZ. (250 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA BODY CLEAR BODY WASH 
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0626
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)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Disodium Cocoamphodiacetate (UNII: 18L9G3U51M)
Glycerin (UNII: PDC6A3C0OX)
Sodium Methyl Cocoyl Taurate (UNII: JVL98CG53G)
Sodium Chloride (UNII: 451W47IQ8X)
Propylene Glycol (UNII: 6DC9Q167V3)
Linoleamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: 5Q87K461JO)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Chamaemelum Nobile Flower (UNII: O2T154T6OG)
Chamomile (UNII: FGL3685T2X)
FD&C Yellow No. 5 (UNII: I753WB2F1M)
D&C Red No. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0626-9	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	01/31/2020

Labeler - Johnson & Johnson Consumer Inc. (002347102)