Active Ingredient

Salicylic Acid 2.0%

Purpose

Anti-dandruff

USE

helps eliminate flaking and irritation

For external use only

When using this product

do not get into 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.

Keep out of reach of children.

If swallowed, get medical
help or contact a Poison Control Center right away.

Directions

■ Apply to affected areas 2 to 4 times daily or as
directed by a doctor. ■ Do not rinse out.

Inactive Ingredients

Water\Aqua\Eau, Alcohol Denat., Betaine,
Sodium Methyl Cocoyl Taurate, Lippia Sidoides (Oregano) Leaf Oil,
Rosmarinus Officinalis (Rosemary) Leaf Extract,
Echinacea Purpurea (Coneflower) Extract, Arctium
Lappa (Burdock) Root Extract, Salvia Officinalis
(Sage) Leaf Extract, Narcissus Tazetta Bulb Extract,
Glycerin, Dimethicone PEG-8 Meadowfoamate,
Hydroxyethylcellulose, Fragrance (Parfum), Eugenol,
Linalool, Citral, Limonene, Sodium Citrate, Sodium
Chloride <ILN45198>

Principal Display Panel

AVEDA
Scalp Remedy
DANDRUFF SOLUTION
helps eliminate flaking and irritation
4.2 fl oz/oz liq/125 ml e PDP

AVEDA SCALP REMEDY DADRUFF
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57677-065
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
LIPPIA SIDOIDES LEAF OIL (UNII: M86P9S87MR)
CITRAL (UNII: T7EU0O9VPP)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
NARCISSUS TAZETTA BULB (UNII: K17762966S)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ECHINACEA PURPUREA (UNII: QI7G114Y98)
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
SAGE (UNII: 065C5D077J)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
EUGENOL (UNII: 3T8H1794QW)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
BETAINE (UNII: 3SCV180C9W)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
ROSEMARY (UNII: IJ67X351P9)
DIMETHICONE PEG-8 MEADOWFOAMATE (UNII: 53UN5B8F4W)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:57677-065-01	125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/06/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M032	12/06/2022	09/10/2024

Labeler - Aveda Corporation (071352058)

Registrant - Estee Lauder Companies Inc. (790802086)

Name	Address	ID/FEI	Business Operations
Establishment
Marietta Corporation dba Voyant Beauty		010765394	manufacture(57677-065)