HEAD AND SHOULDER MEN OLD SPICE- pyrithione zinc lotion/shampoo

HEAD AND SHOULDER by

Drug Labeling and Warnings

HEAD AND SHOULDER by is a Otc medication manufactured, distributed, or labeled by All Natural Dynamics, Procter and Gamble Manufacturara SA De CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DRUGS FACTS

ACTIVE INGREDIENTS

Pyrithione zinc 1%

PURPOSE

PURPOSE

Anti-dandruff

USER SAFETY WARNINGS

USES

Help prevent recurrence of flaking and itching associated with dan druff

WARNINGS

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 procuct as directed.

KEEP OUT OF REACH OF CHILDREN

KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a poison control center rigth away.

DOSAGE & ADMINISTRATION

DIRECTIONS

• for best results use at least twice a week or as directed by doctor.
• for maximun dandruff control, use every time you shampoo
• shake bedore use
• wet hair, message onto scalp, rinse, repeat if desired.

INACTIVE INGREDIENT

WATER, SODIUM LAURYL SULFATE, SODIUM LAURETH SULDATE, GLYCOL DISTEARATE , ZINC CARBONATE, SODIUM CHLORIDE, SODIUM XYLENESULFONATE, COCAMIDOPROPYL BETAINE, FRAGANCE, DIMETHICONE, SODIUM BENZOATE, GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE, MAGNESIUM CARBONATE HYDROXIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1, RED 33

INDICATIONS & USAGE

HELP PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEAD AND SHOULDER  MEN OLD SPICE
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51769-427
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	0.01 mg  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ZINC CARBONATE (UNII: EQR32Y7H0M)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51769-427-01	650 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/10/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	05/10/2022

Labeler - All Natural Dynamics (962732892)

Registrant - All Natural Dynamics (962732892)

Establishment
Name	Address	ID/FEI	Business Operations
Procter and Gamble Manufacturara SA De CV		812807550	manufacture(51769-427)