HEAD AND SHOULDERS DEEP MOISTURE- pyrithione zinc shampoo

Head and Shoulders Deep Moisture by

Drug Labeling and Warnings

Head and Shoulders Deep Moisture 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. Leave on for several minutes. Rinse. Repeat if desired.

Inactive Ingredients

Water, sodium laureth sulfate, cocamideMEA, sodium xylenesulfonate, zinc carbonate, glycol distearate, sodium lauryl sulfate, cocamidopropyl betaine, sodium chloride, fragrance, dimethicone, guar hydroxypropyltrimonium chloride, sodium benzoate, polyquaternium-10, stearyl alcohol, magnesium carbonate hydroxide, cetyl alcohol, persea gratissima (avocado) oil, methylchloroisothiazolinone, methylisothiazolinonee.

Questions (or comments)?

1-800-723-9569

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 380 mL Bottle Label

head &

shoulders ®

pyrithione zince dandruff shampoo

deep moisture

enriched moisture for scalp & hair

with avocado oil

12.8 FL OZ

(380 mL)

INGREDIENTS AND APPEARANCE

HEAD AND SHOULDERS DEEP MOISTURE 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-247
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
POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
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)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CETYL ALCOHOL (UNII: 936JST6JCN)
AVOCADO OIL (UNII: 6VNO72PFC1)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ZINC CARBONATE (UNII: EQR32Y7H0M)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-247-38	380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/01/2017
2	NDC: 69423-247-65	650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/01/2017	07/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	12/01/2017

Labeler - The Procter & Gamble Manufacturing Company (004238200)