Cvs Pharmacy Maximum Strength Dandruff (Selenium Sulfide) Liquid [Cvs Pharmacy] -

CVS PHARMACY MAXIMUM STRENGTH DANDRUFF (SELENIUM SULFIDE) LIQUID [CVS PHARMACY]
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Active ingredient

Selenium Sulfide 1%

Purpose

Anti-dandruff/Anti-seborrheic dermatitis
Uses

for the relief of flaking and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of recurrence.
Warnings
For external use only.
Ask a doctor before use if you have

seborrheic dermatitis in areas other than the scalp.
When using this product
- avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
- for use on color or permed hair, rinse thoroughly.
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.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
- Shake well, apply shampoo and rinse thoroughly.
- for best results, use at least twice a week or as directed by a doctor.
Other information

store at room temperature.
Inactive ingredients

Water (Aqua), Sodium Laureth Sulfate, TEA-Lauryl Sulfate, Cocamidopropyl Betaine, Acrylates Copolymer, Citric Acid, Fragrance, Ammonium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Menthol, Sodium Hydroxide, Magnesium Aluminum Silicate, Hydroxypropyl Methylcellulose, Blue 1 (CI 42090), Red 33 (CI 17200).
Label Copy

INGREDIENTS AND APPEARANCE

CVS PHARMACY MAXIMUM STRENGTH DANDRUFF
selenium sulfide liquid

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q)	SELENIUM SULFIDE	10 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
MENTHOL (UNII: L7T10EIP3A)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:59779-719-11	325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/18/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part358H	07/18/2017

Labeler - CVS Pharmacy (062312574)

Registrant - Apollo Health and Beauty Care Inc. (201901209)

Name	Address	ID/FEI	Business Operations
Establishment
Apollo Health and Beauty Care Inc.		201901209	manufacture(59779-719)

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