DERCOS SALICYLIC ACID ANTI-DANDRUFF SERUM- salicylic acid liquid

Dercos Salicylic Acid Anti-Dandruff Serum by

Drug Labeling and Warnings

Dercos Salicylic Acid Anti-Dandruff Serum by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, PRODUCTOS CAPILARES L'OREAL SA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 1.85%

Purpose

Antidandruff

Uses

• controls the symptoms of dandruff
• fights recurrence of the symptoms of dandruff
• controls scalp itching 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 Center right away.

Directions

• part dry or damp hair in 4 sections
• apply 5 doses to each section
• massage product into scalp
• apply to affected areas one to four times daily or as directed by a doctor 

Inactive ingredients

water, alcohol denat., aminomethyl propanol, ascorbyl glucoside, madecassoside, niacinamide, PEG-40 hydrogenated castor oil, polysorbate 21, sodium hyaluronate, fragrance

Questions or comments?

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERCOS SALICYLIC ACID ANTI-DANDRUFF SERUM 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-892
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	18.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
MADECASSOSIDE (UNII: CQ2F5O6YIY)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
POLYSORBATE 21 (UNII: 59IO08SBZU)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-892-01	1 in 1 CARTON	11/05/2024
1		90 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	11/05/2024

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
PRODUCTOS CAPILARES L'OREAL SA		633333356	manufacture(49967-892)