Active Ingredient

Salicylic Acid 1.8%

Purpose

Anti-Dandruff, Anti-Psoriasis, Anti-Seborrheic Dermatitis

Indications & Usage

Controls flaking, scaling and itching associated with dandruff.

Warnings

For external use only

Do not use

o On scalp that is broken or inflamed

o If you are allergic to ingredients in this product

When using this product

Avoid contact with eyes
If product gets into eyes, rinse thoroughly with water

Stop use and ask a doctor if

Rash appears
Condition worsens or does not improve in 2-4 weeks

Pregnancy or breast feeding

If pregnant or breast-feeding, ask a doctor before use

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Adults and children 12 years ad over	Wet hair thoroughly Apply shampoo, masage into scalp, and rinse thoroughly. Repeat For best results, use at least every other day for 8 weeks or as directed by a doctor. Then use as needed to control dandruff.
Children under 12 years	Ask a doctor

Other information

Store at 20°C to 25°C (68°F-77°F)
See top panel for lot number and expiration date

Inactive ingredients

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl
Hydroxysultaine, Acrylates Copolymer, Glycerin, Propanediol
Caprylate, Polysorbate 80, Niacinamide, Ketoconazole, Curcuma
Longa (Turmeric) Root Extract, Adiantum Capillus-Veneris Leaf
Extract, Thymus Serpyllum Extract, Caprylyl Glycol, 1,2-Hexanediol,
Polyquaternium-7, Amylopectin, Dextrin, Polydextrose, Trisodium
Ethylenediamine Disuccinate, Citric Acid, Sodium Hydroxide,
Hexylene Glycol, Potassium Sorbate, Hydroxyacetophenone,
Ethylhexylglycerin, Sodium Benzoate, Phenoxyethanol

Questions or comments?

Call 1-866-544-3339

Remedy Tube Label v2

REMEDY FOR DANDRUFF
salicylic acid shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:85153-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	18 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
GLYCERIN (UNII: PDC6A3C0OX)
DEXTRIN, POTATO (UNII: ML93R7MDR7)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
THYMUS SERPYLLUM (UNII: 86H4S6K51N)
TURMERIC (UNII: 856YO1Z64F)
AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)
PROPANEDIOL CAPRYLATE (UNII: 7641PCH336)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
KETOCONAZOLE (UNII: R9400W927I)
ADIANTUM CAPILLUS-VENERIS LEAF (UNII: 4817H7M565)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
POLYDEXTROSE (UNII: VH2XOU12IE)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
LUVISET 360 (UNII: 05BG6GY6YK)
NIACINAMIDE (UNII: 25X51I8RD4)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POLYQUATERNIUM-7 (UNII: 0L414VCS5Y)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:85153-001-01	1 in 1 BOX	02/11/2025
1		150 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M032	02/11/2025	06/30/2026

Labeler - Doctorly Skin Inc. (119438421)

Revised: 7/2026

Document Id: 5723a1aa-f67f-eb83-e063-6394a90a637c

Set id: 2cf2a287-1ba8-2d71-e063-6394a90aee5a

Version: 4

Effective Time: 20260721

Doctorly Skin Inc.