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Pantene Pro-V Anti-dandruff

Dosage form: lotion/shampoo
Ingredients: pyrithione zinc 1g in 1mL
Labeler: Procter & Gamble Manufacturing Company
NDC code: 37000-050

PANTENE®
Pro-V®

Drug Facts

Active ingredient

Pyrithione zinc 0.5%

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

wet hair, massage into hair and scalp to create lather. Rinse.
for best results use at least twice a week or as directed by a doctor.

Inactive ingredients

Water, sodium laureth sulfate, sodium lauryl sulfate, glycol distearate, dimethicone, cocamidopropyl betaine, sodium citrate, cocamide mea, sodium xylenesulfonate, fragrance, citric acid, sodium benzoate, guar hydroxypropyltrimonium chloride, benzyl alcohol, sodium chloride, panthenol, panthenyl ethyl ether, methylisothiazolinone.

Questions [or comments]?

1-800-945-7768

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 675 mL Bottle Label

FIGHTS FLAKES, ITCHING,
AND IRRITATION

PANTENE
PRO-V

Pyrithione Zinc
Anti-Dandruff Shampoo

ALL HAIR TYPES

Anti-Dandruff

SHAMPOO

92082231

22.8 FL OZ (675 mL)

PRINCIPAL DISPLAY PANEL - 675 mL Bottle Label

FIGHTS FLAKES, ITCHING,
AND IRRITATION

PANTENE
PRO-V

Pyrithione Zinc
Anti-Dandruff Shampoo & Conditioner

ALL HAIR TYPES

2 IN 1
Anti-Dandruff

SHAMPOO & CONDITIONER

92082224

22.8 FL OZ (675 mL)

PANTENE PRO-V ANTI-DANDRUFF
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37000-050
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
pyrithione zinc (pyrithione zinc)	pyrithione zinc	1 g in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water
sodium laureth-3 sulfate
sodium lauryl sulfate
glycol distearate
dimethicone
cocamidopropyl betaine
sodium citrate
coco monoethanolamide
sodium xylenesulfonate
citric acid monohydrate
sodium benzoate
guar hydroxypropyltrimonium chloride (1.7 substituents per saccharide)
benzyl alcohol
sodium chloride
panthenol
methylisothiazolinone

Packaging
#	Item Code	Package Description
1	NDC:37000-050-37	375 mL in 1 BOTTLE, PLASTIC
2	NDC:37000-050-67	675 mL in 1 BOTTLE, PLASTIC
3	NDC:37000-050-75	750 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part358H	02/01/2012	02/24/2014

PANTENE PRO-V ANTI-DANDRUFF 2IN1
pyrithione zinc lotion/shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37000-051
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
pyrithione zinc (pyrithione zinc)	pyrithione zinc	1 g in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water
sodium laureth-3 sulfate
sodium lauryl sulfate
dimethicone
glycol distearate
cocamidopropyl betaine
sodium citrate
coco monoethanolamide
sodium xylenesulfonate
citric acid monohydrate
sodium benzoate
guar hydroxypropyltrimonium chloride (1.7 substituents per saccharide)
benzyl alcohol
sodium chloride
panthenol
methylisothiazolinone

Packaging
#	Item Code	Package Description
1	NDC:37000-051-37	375 mL in 1 BOTTLE, PLASTIC
2	NDC:37000-051-67	675 mL in 1 BOTTLE, PLASTIC
3	NDC:37000-051-75	750 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part358H	02/01/2012	02/24/2014

Labeler - Procter & Gamble Manufacturing Company (004238200)

Establishment
Name	Address	ID/FEI	Operations
Procter & Gamble Manufacturing Company		005279245	MANUFACTURE(37000-050, 37000-051)

Revised: 12/2013

Document Id: ffe0adf8-e3a0-4478-b577-23eb02ceb4fa

Set id: 0fcdbb02-44fa-4702-af51-de7b52b77578

Version: 2

Effective Time: 20131203

Procter & Gamble Manufacturing Company

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer