DANDRUFF - pyrithione zinc shampoo 
Wal-Mart Stores, Inc

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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Drug Facts

claims

Dry Scalp Control

Pyrithione Zinc

Dandruff Shampoo

Active ingredient

Pyrithione zinc 1%

Purpose

Anti-Dandruff

Use

helps prevent recurrence of flaking and itching associated with dandruff

Warnings

For external use only

When using this product

Stop use and ask a doctor if

Keep out of reach of children

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

Directions

Inactive ingredients

water, sodium lauryl sulfate, sodium laureth,glycol distearate, sodium chloride, zinc carbonate, sodium xylenesulfonate, amodimethicone, cocamidopropyl betaine, fragrance, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, citric acid, Prunus amygdalus dulcis (sweet almond) oil, methylchloroisothiazolinone, methylisothiazolinone

Questions

Call: 1-888-287-1915

guaranteed

Satisfaction guaranteed - For questions or comments please call 1-888-287-1915

adverse reactions

Distributed by: Wal-Mart Stores, Inc.

Bentonville, AR 72716

Disclaimer

This product is not manufactured or distributed by Procter & Gamble, distributor of Head & Shoulders Dry Scalp Care.

Principal display panel

equate

Compare to Head & Shoulders Active Ingredient

Dry Scalp

Control

Pyrithione Zinc

Dandruff Shampoo

23.7 FL OZ (700 mL)

image description

DANDRUFF  
pyrithione zinc shampoo
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-281
Route of Administration TOPICAL DEA Schedule     
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
WATER (UNII: 059QF0KO0R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
sodium chloride (UNII: 451W47IQ8X)  
ZINC CARBONATE (UNII: EQR32Y7H0M)  
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
AMODIMETHICONE (800 CST) (UNII: 363Z2T48P7)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
ALMOND OIL (UNII: 66YXD4DKO9)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49035-281-35 700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 01/05/2009
Labeler - Wal-Mart Stores, Inc (051957769)
Registrant - Vi-Jon (790752542)
Establishment
Name Address ID/FEI Business Operations
Vi-Jon 088520668 manufacture(49035-281)

Revised: 4/2015
Document Id: 4e61e8e5-d372-4e0c-9202-d79c400dffc6
Set id: 4e75d626-bfbe-4d32-941d-3a2992d0beca
Version: 4
Effective Time: 20150415
 
Wal-Mart Stores, Inc