Sebastian Purist Antidandruff Shampoo

Sebastian Purist Antidandruff Shampoo

Drug Labeling and Warnings

Drug Details

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SEBASTIAN PURIST ANTIDANDRUFF- pyrithione zinc shampoo 
THE WELLA CORPORATION

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Sebastian Purist Antidandruff Shampoo

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

inactive ingreds

Questions or comments?

Call 1-800-935-5273

SEB

MAN.

THE PURIST

ANTI-DANDRUFF SHAMPOO

PYRITHIONE ZINC

+Guanana

PROFESSIONAL

SEBASTIAN

250 mL (8.4 FL OZ)

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SEBASTIAN PURIST ANTIDANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69282-008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAFFEINE (UNII: 3G6A5W338E)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PEG-3 DISTEARATE (UNII: 8420ECX438)  
SODIUM LAURETH-8 SULFATE (UNII: YP8U3694P0)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ALLANTOIN (UNII: 344S277G0Z)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
PANTHENOL (UNII: WV9CM0O67Z)  
MAGNESIUM LAURETH SULFATE (UNII: UKW9G007TZ)  
MAGNESIUM LAURETH-8 SULFATE (UNII: 2OTJ9LF5UA)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69282-008-10250 mL in 1 BOTTLE; Type 0: Not a Combination Product06/27/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H06/27/2019
Labeler - THE WELLA CORPORATION (829413157)
Registrant - COTY US LLC (039056361)

Revised: 6/2019
 
THE WELLA CORPORATION


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