HEAD AND SHOULDERS DRY SCALP CARE- pyrithione zinc lotion/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 ®

Dry Scalp Care

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, prunus amygdalus dulcis (sweet almond) oil, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 835mL Bottle Label

head &
shoulders ®

pyrithione zinc dandruff shampoo

DRY SCALP CARE
Daily Shampoo


CLINICALLY PROVEN TO HELP
RESTORE SCALP'S NATURAL MOISTURE
INFUSED WITH ALMOND OIL

FLAKE FREE.*

UP TO 100%

GUARANTEED^

28.2 FL OZ (835 mL)

HS

HEAD AND SHOULDERS  DRY SCALP CARE
pyrithione zinc lotion/shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-092
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
DIMETHICONOL GUM (UNII: 4MJ9GU3T1P)  
TRIDECETH-10 (UNII: G624N6MSBA)  
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)  
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ZINC CARBONATE (UNII: EQR32Y7H0M)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)  
ALMOND OIL (UNII: 66YXD4DKO9)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-092-70700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/201310/05/2018
2NDC:37000-092-101000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/201310/05/2018
3NDC:37000-092-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/22/201401/01/2025
4NDC:37000-092-25250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/30/201504/01/2023
5NDC:37000-092-95950 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/01/201601/01/2025
6NDC:37000-092-71700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/23/201801/01/2025
7NDC:37000-092-012 in 1 CELLO PACK07/15/2020
7950 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
8NDC:37000-092-37370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2022
9NDC:37000-092-61613 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2022
10NDC:37000-092-83835 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM03209/01/2013
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 2/2023
Document Id: f5c6a34f-d9fa-b672-e053-2a95a90add31
Set id: ac6ea4ae-623c-4f45-841c-a168d51d7068
Version: 11
Effective Time: 20230228
 
The Procter & Gamble Manufacturing Company