DANDRUFF SHAMPOO- pyrithione zinc lotion/shampoo

Dandruff Shampoo by

Drug Labeling and Warnings

Dandruff Shampoo by is a Otc medication manufactured, distributed, or labeled by Cardinal Health, Vi Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                      Purpose

Pyrithione Zinc   1%                          Anti-Dandruff

INDICATIONS & USAGE

Use  helps prevent recurrence of flaking and itching associated with dandruff

WARNINGS

Warnings
For external use only

When using this product
do not get into 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 as directed

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions
shake well for maximum dandruff control, use every time you shampoo wet hair, message onto scalp, rinse, repeat if desired
for best result use at least twice a week or as directed by doctor

INACTIVE INGREDIENT

Inactive ingredients water, sodium laureth sulfate, glycol distearate, sodium lauryl sulfate, cocamidopropyl betaine, cocamide MEA,
zinc carbonate, behentrimonium chloride, fragrance, magnesium sulfate, sodium benzoate, zinc chloride, sodium citrate, benzyl alcohol, sodium chloride, sodium hydroxide, blue 1, red 4

PRINCIPAL DISPLAY PANEL

Compare to
Head + Shoulders
active ingredient
Pyrithione Zinc
Dandruff
Shampoo
Everyday Clean
Everyday basi cleaning
for Normal or Oily Hair
14.2 FL OZ
(420 mL)

INGREDIENTS AND APPEARANCE

DANDRUFF SHAMPOO 
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37205-311
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 kg  in 100 L

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ZINC CARBONATE (UNII: EQR32Y7H0M)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ZINC (UNII: J41CSQ7QDS)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37205-311-15	.42 L in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358	05/19/1998

Labeler - Cardinal Health (097537435)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture