OUAI ANTI-DANDRUFF- salicylic acid shampoo

Ouai Anti-Dandruff by

Drug Labeling and Warnings

Ouai Anti-Dandruff by is a Otc medication manufactured, distributed, or labeled by United Beauty Brands, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

Salicylic Acid 2%

Purpose

Anti-Dandruff

Use

Reduces scalp flaking, itching, and irritation associated with dandruff

Warnings

For external use only

When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.

Keep out of reach of children. If swallowed, get medical help or contact a poison control right away.

Directions

• Apply to wet hair and massage into scalp.
• Leave on for 5 minutes and rinse thoroughly.
• For best results use at least twice a week or as directed by a doctor.

Inactive Ingredients

Water, Cocamidopropyl Betaine, Sodium C14-16 Olefin Sulfonate, Glycerin, Sodium Lauroyl Methyl Isethionate, Polysorbate 80, Acrylates Copolymer, Propanediol Caprylate, Potassium Hydroxide, Sodium Benzoate, Sodium Methyl Oleoyl Taurate, Sodium Cocoyl Isethionate, Cocamide MIPA, Cassia Hydroxypropyltrimonium Chloride, Polyquaternium-113, Chlorphenesin, Tetrasodium EDTA, Silicone Quaternium-22, Dipropylene Glycol, Epilobium Angustifolium Flower/Leaf/Stem Extract, Polyglyceryl-3 Caprate, PEG-45M, Citric Acid, Fragrance.

Questions or comments

team@theouai.com

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DIST. BY OUAI BEVERLY HILLS,
CA 90210 USA

PRINCIPAL DISPLAY PANEL - 300 ml Bottle Label

OUAI

ANTI-DANDRUFF SHAMPOO

2% SALICYLIC ACID

10 fl oz / 300 ml

INGREDIENTS AND APPEARANCE

OUAI ANTI-DANDRUFF 
salicylic acid shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83058-0140
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	2 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Glycerin (UNII: PDC6A3C0OX)
Sodium Lauroyl Methyl Isethionate (UNII: II6VCD3S6R)
Polysorbate 80 (UNII: 6OZP39ZG8H)
Acrylates Crosspolymer-4 (UNII: GEV2EL4D9G)
Propanediol Caprylate (UNII: 7641PCH336)
Potassium Hydroxide (UNII: WZH3C48M4T)
Sodium Benzoate (UNII: OJ245FE5EU)
Sodium Methyl Oleoyl Taurate (UNII: 8PZ076134H)
Sodium Cocoyl Isethionate (UNII: 518XTE8493)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
Chlorphenesin (UNII: I670DAL4SZ)
EDETATE SODIUM (UNII: MP1J8420LU)
Dipropylene Glycol (UNII: E107L85C40)
EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
Polyglyceryl-3 Caprate (UNII: VZQ347QQ3H)
POLYETHYLENE OXIDE 2000000 (UNII: 5K3991GVWI)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83058-0140-1	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/17/2022
2	NDC: 83058-0140-4	30 mL in 1 TUBE; Type 0: Not a Combination Product	11/17/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M032	11/17/2022

Labeler - United Beauty Brands, LLC (080321665)