HEAD AND SHOULDERS SUPREME COLOR PROTECT- pyrithione zinc shampoo

Head and Shoulders Supreme Color Protect by

Drug Labeling and Warnings

Head and Shoulders Supreme Color Protect 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 laureth sulfate, zinc carbonate, glycol distearate, cocamide MEA, cocamidopropyl betaine, sodium xylenesulfonate, sodium chloride, dimethicone, argania spinosa kernel oil, honey extract, fragrance, guar hydroxypropyltrimonium chloride, sodium benzoate, polyquaternium-10, stearyl alcohol, magnesium carbonate hydroxide, cetyl alcohol, methylchloroisothiazolinone, methylisothiazolinone

Questions (or comments)?

1-800-723-9569

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 350 mL Bottle Label

head &
shoulders ®
PYRITHIONE ZINC DANDRUFF

SCALP & HAIR SHAMPOO

SUPREME

COLOR

PROTECT

WITH ARGAN OIL

& MANUKA HONEY

FREE FROM

PHOSPHATES

PARABENS

PHTHALATES

DYES

11.8 FL OZ
(350 mL)

INGREDIENTS AND APPEARANCE

HEAD AND SHOULDERS SUPREME COLOR PROTECT 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-346
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
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
WATER (UNII: 059QF0KO0R)
CETYL ALCOHOL (UNII: 936JST6JCN)
ZINC CARBONATE (UNII: EQR32Y7H0M)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
HONEY (UNII: Y9H1V576FH)
DIMETHICONE (UNII: 92RU3N3Y1O)
ARGAN OIL (UNII: 4V59G5UW9X)
POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-346-35	350 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/02/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	05/02/2019

Labeler - The Procter & Gamble Manufacturing Company (004238200)