HEAD AND SHOULDERS DEEP SCALP HYDRATION DAILY- pyrithione zinc shampoo

Head and Shoulders Deep Scalp Hydration Daily by

Drug Labeling and Warnings

Head and Shoulders Deep Scalp Hydration Daily by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

• for best results use at least twice a week or as directed by a doctor.
• for maximum dandruff control, use every time you shampoo.
• shake before use.
• wet hair, massage onto scalp, rinse, repeat if desired.

Inactive ingredients

Water, sodium lauryl sulfate, glycol distearate, zinc carbonate, sodium chloride, fragrance, cocamidopropyl betaine, sodium xylenesulfonate, dimethicone, sodium benzoate, guar hydroxypropyltrimonium chloride, stearyl stearate,magnesium carbonate hydroxide, sodium laureth sulfate, euphorbia cerifera (candelilla) wax, jojoba esters, ferric ammonium ferrocyanide

Questions (or comments)?

1-800-723-9569

SPL UNCLASSIFIED SECTION

MADE IN U.S.A. of U.S. and/or Imported Ingredients

Dist. by PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 370 mL Bottle Label

head &
shoulders ®

PYRITHIONE ZINC DANDRUFF SHAMPOO

DEEP SCALP

HYDRATION

DAILY SHAMPOO

Deeply cleans & seals

in scalp moisture

with naturally-derived exfoliants

12.5 FL OZ (370 mL)

INGREDIENTS AND APPEARANCE

HEAD AND SHOULDERS DEEP SCALP HYDRATION DAILY 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-672
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
JOJOBA OIL (UNII: 724GKU717M)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
ZINC CARBONATE (UNII: EQR32Y7H0M)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CANDELILLA WAX (UNII: WL0328HX19)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
FERRIC AMMONIUM FERROCYANIDE (UNII: 9R0NVI936I)
STEARYL STEARATE (UNII: 5WX2EGD0DK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-672-37	370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/15/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	12/15/2022

Labeler - The Procter & Gamble Manufacturing Company (004238200)