PYRITHIONE ZINC 0.5 DANDRUFF- pyrithione zinc shampoo 
Universal Distribution Center LLC

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Dandruff SHAMPOO ALL HAIR TYPES

Drug Facts

Active Ingredient:

Pyrithione zinc 0.5% W/V

Purpose:

Anti-dandruff

Uses:

Helps prevent recurrence of flaking and itching associated with dandruff.

Directions:

Wet hair, massage onto scalp, rinse. Repeat if desired. For best results use at least twice a week or as directed by a doctor.

Other Information:

Store at 20°C to 25°C (68°F to 77°F)

Inactive Ingredients:

Water, Sodium Lauryl Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Cocamide Mea, Acrylated Co Polymer, Glycerin, Fragrance, Citric Acid, Disodium Edta, Aloe Barbadensis Leaf Juice, Methylchloroisothiazolinone, Methylisothiazolinone, Guar Hydroxypropyltrimonium Chloride, Glycol Distearate, Menthol, Fd & C Blue No.1

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. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children.

ALL HAIR TYPES

Helps to relieve itching, dryness and flakes

Distributed by:
Universal Distribution Center LLC
96 Distribution Boulevard, Edison, NJ 08817
www.universaldc.com

Made in India                                                                           

Packaging

Anti-Dandruff

PYRITHIONE ZINC 0.5 DANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-416
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
GLYCERIN (UNII: PDC6A3C0OX)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-416-12355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/17/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03205/17/2024
Labeler - Universal Distribution Center LLC (019180459)

Revised: 4/2024
Document Id: 525340f0-03e9-4919-a006-c9b0f48df553
Set id: bb8128e0-c589-4ac6-902a-322d3ab6d512
Version: 1
Effective Time: 20240429
 
Universal Distribution Center LLC