QUALITY CHOICE DANDRUFF DRY SCALP CARE- pyrithione zinc lotion/shampoo

Quality Choice Dandruff Dry Scalp Care by

Drug Labeling and Warnings

Quality Choice Dandruff Dry Scalp Care by is a Otc medication manufactured, distributed, or labeled by CHAIN DRUG MARKETING ASSOCIATION, INC., Medical Group Care LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Pyrithione zinc

Purpose

Antidandruff

Use

helps prevent recurrence of scalp flaking and 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

• shake before use
• wet hair, massage onto scalp, rinse and repeat if desired
• for best results use at least twice a week or as directed by a doctor
• for maximum dandruff control, use every time when you want to shampoo

Other information

store away from direct sunlight, excessive heat, and freezing conditions

Inactive ingredients

water, sodium laureth sulfate, cocamidopropyl betaine, glycol distearate, acrylates copolymer, styrene/acrylates copolymer, polyquaternium-7, propylene glycol, sodium lauryl sulfate, cocamide MEA, silicone quaternium-16, phenoxyethanol, fragrance, sodium chloride, polyquaternium-10, trideceth-12, glycerin, ethylhexylglycerin, menthol, sweet almond (Prunus amygdalus dulcis) oil, hydroxyacetophenone, caramel, FD&C yellow no. 5

Questions?

+1-800-935-2362
You may also report serious side effects to this phone number.
Monday-Friday 9AM-5PM EST

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QUALITY CHOICE DANDRUFF DRY SCALP CARE 
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-322
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
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL (UNII: 66YXD4DKO9)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
POLYQUATERNIUM-7 (UNII: 0L414VCS5Y)
QUATERNIUM-16 (UNII: K4H0FG9I2T)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
TRIDECETH-12 (UNII: YFY3KG5Y7O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
MENTHOL (UNII: L7T10EIP3A)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDE MEA (UNII: C80684146D)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARAMEL (UNII: T9D99G2B1R)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-322-13	399 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	01/23/2025

Labeler - CHAIN DRUG MARKETING ASSOCIATION, INC. (011920774)

Registrant - Medical Group Care LLC (085137089)