HEAD AND SHOULDERS COCONUT DAILY HAIR AND SCALP CONDITIONER- pyrithione zinc lotion 
The Procter & Gamble Manufacturing Company

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 and Shoulders ® Coconut Hair and Scalp Conditioner

Drug Facts

Active ingredient

Pyrithione zinc 0.5%

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, stearyl alcohol, cetyl alcohol, stearamidopropyl dimethylamine, glutamic acid, dimethicone, fragrance, phenoxyethanol, benzyl alcohol, citric acid, sodium chloride, zea mays (corn) silk extract, orchis mascula flower extract, cocos nucifera (coconut) fruit extract, methylchloroisothiazolinone, methylisothiazolinone.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 325 mL Tube Label

head &
shoulders ®

pyrithione zinc dandruff conditioner

COCONUT

DAILY HAIR & SCALP

CONDITIONER

restores hair & scalp

moisture

infused with coconut milk

10.9 FL OZ (325 mL)

HS

HEAD AND SHOULDERS COCONUT  DAILY HAIR AND SCALP CONDITIONER
pyrithione zinc lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-319
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 0.5 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
ORCHIS MASCULA FLOWER (UNII: 6H1JQK35LA)  
COCONUT (UNII: 3RT3536DHY)  
WATER (UNII: 059QF0KO0R)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)  
GLUTAMIC ACID (UNII: 3KX376GY7L)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CORN SILK (UNII: 7D3VB244UX)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:69423-319-32 325 mL in 1 TUBE; Type 0: Not a Combination Product 11/29/2018
2 NDC:69423-319-25 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/04/2018
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 11/29/2018
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 12/2018
Document Id: 7d3f8f47-98e9-7f68-e053-2991aa0a02da
Set id: 7cc10c1b-fe0b-7d4c-e053-2a91aa0a2377
Version: 2
Effective Time: 20181217
 
The Procter & Gamble Manufacturing Company