CVS ANTI DANDRUFF- pyrithione zinc shampoo

CVS ANTI DANDRUFF by

Drug Labeling and Warnings

CVS ANTI DANDRUFF 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

Pyrithione Zinc (1%)

Purpose

Anti-dandruff.

Uses

Controls the symptoms of dandruff.

Warnings

For external use only

When using this product

avoid contact with eyes. If contact occurs, rise eyes thoroughly with water.

Stop use and ask a doctor if

condition worsen 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 Comtrol Center immediately.

Directions

• for best results, use at least twice weekly or as directed by the physician.
• Apply to wet skin and/or scalp and massage to form a lather.
• Leave lather on for few minutes.
• Rinse thoroughly and repeat if necessary.

Inactive Ingredients

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Cocamide MIPA, Glycol Stearate, Acrylates Copolymer, Amodimethicone, Tocopherol, Ceramide AP, Ceramide EOP, Ceramide NP, Niacinamide, Phytospingosine, Chlesterol, Sodium Hyaluronate, Polyquaternium-10, Carbomer, Cetrimonium Chloride, Trideceth-12, Coco-Betaine, Disodium Laureth Sulfosuccinate, Ethylhexylglycerin, Benzyl Alcohol, Sodium Hydroxide, Potato Starch Modified, PPG-5-Ceteth-20, Sodium Lauroyl Lactylate, Sodium Lauryl Sulfoacetate, Salicylic Acid, Xanthan Gum.

Principal Display Panel

INGREDIENTS AND APPEARANCE

CVS ANTI DANDRUFF 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63148-212
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCO-BETAINE (UNII: 03DH2IZ3FY)
CERAMIDE 9 (UNII: 88KCS7120E)
WATER (UNII: 059QF0KO0R)
POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COCAMIDE MIPA (UNII: 21X4Y0VTB1)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
GLYCOL STEARATE (UNII: 0324G66D0E)
SALICYLIC ACID (UNII: O414PZ4LPZ)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
NIACINAMIDE (UNII: 25X51I8RD4)
CERAMIDE AP (UNII: F1X8L2B00J)
CERAMIDE NP (UNII: 4370DF050B)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CHOLESTEROL (UNII: 97C5T2UQ7J)
TOCOPHEROL (UNII: R0ZB2556P8)
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
TRIDECETH-12 (UNII: YFY3KG5Y7O)
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C)
SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
AMODIMETHICONE (240 CST) (UNII: VA5T401RWV)
CARBOMER (UNII: 0A5MM307FC)
XANTHAN GUM (UNII: TTV12P4NEE)
STARCH, POTATO (UNII: 8I089SAH3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63148-212-12	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	10/01/2025

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(63148-212)