Head and Shoulders ® Scalp X Shampoo for Men

Head and Shoulders Scalp X for Men by

Drug Labeling and Warnings

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

Drug Details [pdf]

HEAD AND SHOULDERS SCALP X FOR MEN- pyrithione zinc shampoo 
The Procter & Gamble Manufacturing Company

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Head and Shoulders ® Scalp X Shampoo for Men

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, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, dimethicone, sodium xylenesulfonate, cocamidopropyl betaine, fragrance, sodium benzoate, menthol, guar hydroxypropyltrimonium chloride, magnesium
carbonate hydroxide, mentha piperita (peppermint) oil, mentha arvensis leaf oil, tocopheryl acetate, methylchloroisothiazolinone, methylisothiazolinone.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 150 mL Bottle label

head &
shoulders ®

PYRITHIONE ZINC

DANDRUFF SHAMPOO

SCALP X

SHAMPOO

FOR MEN

REDUCES HAIR LOSS

DUE TO BREAKAGE

5 FL OZ (150 mL)

HEAD AND SHOULDERS SCALP X FOR MEN 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-644
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 LAURYL SULFATE (UNII: 368GB5141J)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
MENTHOL (UNII: L7T10EIP3A)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
PEPPERMINT OIL (UNII: AV092KU4JH)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ZINC CARBONATE (UNII: EQR32Y7H0M)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-644-15	150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/01/2022	09/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	09/01/2022	09/01/2024

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 12/2023

Document Id: 0c92d0b3-1764-de2d-e063-6394a90a34d1

34390-5

Set id: ecf8c4d8-f44d-616f-e053-2995a90a304e

Version: 2

Effective Time: 20231215

 

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