HEAD AND SHOULDERS  DRY SCALP- pyrithione zinc lotion/shampoo 
Procter & Gamble Manufacturing Co

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.

----------

head & shoulders®
pyrithione zinc
dandruff shampoo

Drug Facts

Active ingredient

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 this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

water, sodium laureth sulfate, sodium lauryl sulfate, cocamide MEA, zinc carbonate, glycol distearate, dimethicone, fragrance, cetyl alcohol, polyquaternium-10, magnesium sulfate, sodium benzoate, magnesium carbonate hydroxide, ammonium laureth sulfate, benzyl alcohol, sodium chloride, methylchloroisothiazolinone, methylisothiazolinone, sodium xylenesulfonate.

Questions (or comments)?

1-800-723-9569

www.headandshoulders.com
Made in U.S.A. of US and/or imported ingredients.
Dist. by Procter & Gamble, Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 420mL Bottle Label

head &
shoulders®

pyrithione zinc
dandruff shampoo

IMPROVES HAIR & SCALP
HEALTH GUARANTEED

dry scalp care
with moisturizers,
relieves dry scalp and itch

14.2 FL OZ (420mL)

Principal Display Panel - 420mL Bottle Label
HEAD AND SHOULDERS   DRY SCALP
pyrithione zinc lotion/shampoo
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:37000-781
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Pyrithione Zinc (Pyrithione Zinc) Pyrithione Zinc1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
sodium laureth-3 sulfate 
sodium lauryl sulfate 
Coco Monoethanolamide 
zinc carbonate 
glycol distearate 
dimethicone 
cetyl alcohol 
magnesium sulfate 
sodium benzoate 
magnesium carbonate hydroxide 
benzyl alcohol 
sodium chloride 
methylchloroisothiazolinone 
methylisothiazolinone 
sodium xylenesulfonate 
Product Characteristics
ColorTURQUOISEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-781-14420 mL in 1 BOTTLE, PLASTIC
2NDC:37000-781-23700 mL in 1 BOTTLE, PLASTIC
3NDC:37000-781-331000 mL in 1 BOTTLE, PLASTIC
4NDC:37000-781-401180 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H01/01/200602/24/2016
Labeler - Procter & Gamble Manufacturing Co (004238200)

Revised: 6/2014
Document Id: e39f97b8-f3ac-4644-9f57-e4957a3e9ac4
Set id: c23dc070-87f4-480f-b04b-967e42462ddb
Version: 4
Effective Time: 20140619
 
Procter & Gamble Manufacturing Co