Head and Shoulders ® Scalp X Shampoo

Head and Shoulders Scalp X by

Drug Labeling and Warnings

Head and Shoulders Scalp X 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- pyrithione zinc shampoo 
The Procter & Gamble Manufacturing Company

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Head and Shoulders ® Scalp X 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

• 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

REDUCES HAIR LOSS

DUE TO BREAKAGE

with Vitamin E

5 FL OZ (150 mL)

HEAD AND SHOULDERS SCALP X 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-643
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
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
PEPPERMINT OIL (UNII: AV092KU4JH)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
ZINC CARBONATE (UNII: EQR32Y7H0M)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-643-15	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)

Establishment
Name	Address	ID/FEI	Business Operations
The Procter & Gamble Manufacturing Company		081329183	manufacture(69423-643) , pack(69423-643)

Revised: 12/2023

Document Id: 0c92b8c4-4cff-5478-e063-6294a90a7c3e

34390-5

Set id: ecf77aae-8216-f2bb-e053-2995a90a74f2

Version: 2

Effective Time: 20231215

 

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