CVS GOLD- selenium sulfide shampoo

CVS Gold by

Drug Labeling and Warnings

CVS Gold by is a Otc medication manufactured, distributed, or labeled by Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Selenium Sulfide 1%

Purpose

Anti-dandruff Anti-seborrheic dermatitis

Uses

Helps prevent recurrence of flaking and itching associated with dandruff and seborrheic dermatitis.

Warnings

For external use only

Ask a doctor before use if you havea condition that covers a large area of the body.

When using this productavoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor ifcondition 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

• Apply a generous amount to wet hair, massage onto scalp and work evenly to the ends.
• Leave on for 3-5 minutes.
• Rinse thoroughly.
• For best results use at least twice a week or as directed by a doctor.

Inactive Ingredients

Acrylate Copolymer, Caprylyl Glycol, Citric Acid, Cocamidopropyl Betaine, Dimethicone, Fragrance (Parfum), Glycol Stearate, Honey, Hydroxypropyl Methylcellulose, Phenoxyethanol, Red 4 (CI 14700), Sodium Chloride, Sodium Citrate, Sodium Hydroxide, Sodium Laureth Sulfate, Tetrasodium EDTA, Water (Aqua).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS GOLD 
selenium sulfide shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63148-209
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q)	SELENIUM SULFIDE	1000 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID (UNII: 2968PHW8QP)
DIMETHICONE (UNII: 92RU3N3Y1O)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
TETRASODIUM EDTA (UNII: MP1J8420LU)
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C)
HONEY (UNII: Y9H1V576FH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCOL STEARATE (UNII: 0324G66D0E)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
HYDROXYPROPYL METHYLCELLULOSE (UNII: 3NXW29V3WO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63148-209-13	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	12/02/2024

Labeler - Apollo Health and Beauty Care (201901209)

Registrant - Apollo Health and Beauty Care (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care		201901209	manufacture(63148-209)