HEAD AND SHOULDERS CLASSIC CLEAN DANDRUFF- pyrithione zinc shampoo

Head and Shoulders Classic Clean Dandruff by

Drug Labeling and Warnings

Head and Shoulders Classic Clean Dandruff by is a Otc medication manufactured, distributed, or labeled by Navajo Manufacturing Company Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

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 the 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, zinc carbonate, sodium chloride, sodium xylenesulfonate, cocamidopropyl betaine, fragrance, dimethicone, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

Questions or comments?

1-800-723-9569

Head & Shoulders Classic Clean Dandruff Shampoo 50ml (

67751-053-01)

INGREDIENTS AND APPEARANCE

HEAD AND SHOULDERS CLASSIC CLEAN DANDRUFF 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67751-053(NDC:37000-071)
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
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
ZINC CARBONATE (UNII: EQR32Y7H0M)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67751-053-01	1 in 1 CARTON	11/10/2017
1		50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	05/31/2013

Labeler - Navajo Manufacturing Company Inc (091917799)

Establishment
Name	Address	ID/FEI	Business Operations
The Procter & Gamble Manufacturing Company		007130032	manufacture(67751-053)

Establishment
Name	Address	ID/FEI	Business Operations
Navajo Manufacturing Company Inc		136941411	relabel(67751-053) , repack(67751-053)