SEBASTIAN PURIST ANTIDANDRUFF- pyrithione zinc shampoo

Sebastian Purist Antidandruff by

Drug Labeling and Warnings

Sebastian Purist Antidandruff by is a Otc medication manufactured, distributed, or labeled by THE WELLA CORPORATION, COTY US LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Pyrithione Zinc 1%

Purpose

Anti-dandruff

Uses

Helps prevent recurrence of flaking and itching associated with dandruff

Warnings

For external use only.

When using this product

avoid contact with 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.

Directions

For best results use at least twice a week or as directed by a doctor.Apply a small amount evenly over wet scalp and hair. Leave on for several minutes. Rinse well.

Inactive ingredients

Questions or comments?

Call 1-800-935-5273

PRINCIPAL DISPLAY PANEL

SEB

MAN.

THE PURIST

ANTI-DANDRUFF SHAMPOO

PYRITHIONE ZINC

+Guanana

PROFESSIONAL

SEBASTIAN

250 mL (8.4 FL OZ)

INGREDIENTS AND APPEARANCE

SEBASTIAN PURIST ANTIDANDRUFF 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69282-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAFFEINE (UNII: 3G6A5W338E)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM SULFITE (UNII: VTK01UQK3G)
PEG-3 DISTEARATE (UNII: 8420ECX438)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAURETH-8 SULFATE (UNII: YP8U3694P0)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALLANTOIN (UNII: 344S277G0Z)
METHYLPARABEN (UNII: A2I8C7HI9T)
MAGNESIUM LAURETH SULFATE (UNII: UKW9G007TZ)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PANTHENOL (UNII: WV9CM0O67Z)
MAGNESIUM LAURETH-8 SULFATE (UNII: 2OTJ9LF5UA)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69282-008-10	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/27/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	06/27/2019

Labeler - THE WELLA CORPORATION (829413157)

Registrant - COTY US LLC (039056361)