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.

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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 Type HUMAN OTC DRUG Item Code (Source) NDC:37000-781
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 1 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
water (UNII: 059QF0KO0R)  
sodium laureth-3 sulfate (UNII: BPV390UAP0)  
sodium lauryl sulfate (UNII: 368GB5141J)  
Coco Monoethanolamide (UNII: C80684146D)  
zinc carbonate (UNII: EQR32Y7H0M)  
glycol distearate (UNII: 13W7MDN21W)  
dimethicone (UNII: 92RU3N3Y1O)  
cetyl alcohol (UNII: 936JST6JCN)  
magnesium sulfate (UNII: DE08037SAB)  
sodium benzoate (UNII: OJ245FE5EU)  
magnesium carbonate hydroxide (UNII: YQO029V1L4)  
benzyl alcohol (UNII: LKG8494WBH)  
sodium chloride (UNII: 451W47IQ8X)  
methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
methylisothiazolinone (UNII: 229D0E1QFA)  
sodium xylenesulfonate (UNII: G4LZF950UR)  
Product Characteristics
Color TURQUOISE Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37000-781-14 420 mL in 1 BOTTLE, PLASTIC
2 NDC:37000-781-23 700 mL in 1 BOTTLE, PLASTIC
3 NDC:37000-781-33 1000 mL in 1 BOTTLE, PLASTIC
4 NDC:37000-781-40 1180 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 01/01/2006 02/24/2016
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