VICHY LABORATOIRES DERCOS SELENIUM SULFIDE ANTI-DANDRUFF- selenium sulfide, micronized shampoo

VICHY LABORATOIRES DERCOS Selenium Sulfide Anti-Dandruff by

Drug Labeling and Warnings

VICHY LABORATOIRES DERCOS Selenium Sulfide Anti-Dandruff 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

Selenium sulfide, micronized 0.6%

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

• for best results, use at least twice a week or as directed by a doctor
• shake well
• wet hair and apply small amount of shampoo
• massage vigorously
• leave on for 2 minutes
• rinse well

Inactive ingredients

water, sodium laureth sulfate, glycol distearate, dimethicone, coco-betaine, sodium lauryl sulfate, glycerin, carbomer, citric acid, menthol, niacinamide, PPG-5-ceteth-20, salicylic acid, sodium benzoate, sodium chloride, sodium hydroxide, yellow 10, fragrance

Questions or comments?

1-877-378-4249

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INGREDIENTS AND APPEARANCE

VICHY LABORATOIRES DERCOS SELENIUM SULFIDE ANTI-DANDRUFF 
selenium sulfide, micronized shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-974
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q)	SELENIUM SULFIDE	6 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
DIMETHICONE (UNII: 92RU3N3Y1O)
COCO-BETAINE (UNII: 03DH2IZ3FY)
Sodium Lauryl Sulfate (UNII: 368GB5141J)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
MENTHOL (UNII: L7T10EIP3A)
NIACINAMIDE (UNII: 25X51I8RD4)
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
SALICYLIC ACID (UNII: O414PZ4LPZ)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-974-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	10/01/2024
2	NDC: 49967-974-02	1 in 1 CARTON	10/01/2024
2		200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 49967-974-03	390 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	10/01/2024

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
PRODUCTOS CAPILARES L'OREAL SA		633333356	manufacture(49967-974)