NEUTROGENA OIL FREE ACNE WASH- salicylic acid liquid

Neutrogena Oil Free Acne Wash by

Drug Labeling and Warnings

Neutrogena Oil Free Acne Wash 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 Room Temperature.

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, PEG-80 Sorbitan Laurate, Citric Acid, Disodium EDTA, C12-15 Alkyl Lactate, Benzalkonium Chloride, Fragrance, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerin, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Propylene Glycol, Sodium Hydroxide, Yellow 5, Red 40

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 - 269 mL Bottle Label

Oil-Free

Acne Wash

MICRO CLEAR ®

technology

DERMATOLOGIST RECOMMENDED

Neutrogena ®

salicylic acid acne treatment

9.1 FL. OZ. (269 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA OIL FREE ACNE WASH 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0770
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)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PEG-80 SORBITAN LAURATE (UNII: 239B50Y732)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMOMILE (UNII: FGL3685T2X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0770-1	12 in 1 TRAY	07/29/2022
1		14 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69968-0770-6	177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/29/2022
3	NDC: 69968-0770-9	269 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/29/2022
4	NDC: 69968-0770-2	2 in 1 CARTON	07/29/2022
4		269 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	07/29/2022

Labeler - Kenvue Brands LLC (118772437)