HEAD AND SHOULDERS COCONUT DAILY- pyrithione zinc shampoo 
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 Daily 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, cocamidopropyl betaine, sodium xylenesulfonate, zinc carbonate, glycol distearate, fragrance, sodium chloride, dimethiconol, sodium benzoate, guar hydroxypropyltrimonium chloride, dimethicone, TEA-dodecylbenzenesulfonate, magnesium carbonate hydroxide, trideceth-10, zea mays (corn) silk extract, cocos nucifera (coconut) fruit extract, benzyl alcohol,methylchloroisothiazolinone,methylisothiazolinone, yellow 5, red 33, blue 1

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 370 mL Bottle Label

head &
shoulders ®

pyrithione zinc dandruff shampoo

COCONUT

DAILY SHAMPOO

RESTORES HAIR & SCALP MOISTURE

INFUSED WITH COCONUT MILK

12.5 FL OZ (370 mL)

HS

HEAD AND SHOULDERS COCONUT DAILY 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-315
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
CORN SILK (UNII: 7D3VB244UX)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
COCONUT (UNII: 3RT3536DHY)  
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ZINC CARBONATE (UNII: EQR32Y7H0M)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
DIMETHICONOL GUM (UNII: 4MJ9GU3T1P)  
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)  
TRIDECETH-10 (UNII: G624N6MSBA)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-315-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/29/201812/01/2024
2NDC:69423-315-25250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/29/201812/01/2024
3NDC:69423-315-37370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM03211/29/2018
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 3/2023
Document Id: f5f305df-f7ed-079e-e053-2995a90adc99
Set id: 7cc1500e-b278-140a-e053-2991aa0ae6f2
Version: 6
Effective Time: 20230302
 
The Procter & Gamble Manufacturing Company