AXE FREEZE ANTIDANDRUFF- pyrithione zinc shampoo

Axe by

Drug Labeling and Warnings

Axe by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a Unilever, Unilever Supply Chain Co. d/b/a Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient
Pyrithione Zinc (1.0%)

PURPOSE

Purpose

Anti-dandruff

INDICATIONS & USAGE

Use helps control scalp itching and flaking associated with dandruff.

WARNINGS

Warnings
For external use only

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center Right Away.

Avoid contact with eyes.  Product contains menthol.  If you experience discomfort, please stop use.

Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.

DOSAGE & ADMINISTRATION

Direction

·  Squeeze. Lather. Rinse
·  For best results, use at least twice a week or as directed by a doctor.

INACTIVE INGREDIENT

Inactive ingredients
Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Fragrance (Parfum), Carbomer, Dimethiconol, Menthol, DMDM Hydantoin, Citric Acid, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, Propylene Glycol, PPG-9, Methylisothiazolinone, Methylchloroisothiazolinone, Blue 1 (CI 42090), Yellow 5 (CI 19140).

QUESTIONS

theaxeeffect.com
QUESTIONS/COMMENTS?
1-800-450-7580

12 FL OZ PDP

12 FL OZ back

INGREDIENTS AND APPEARANCE

AXE  FREEZE ANTIDANDRUFF
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1357
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 LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
MENTHOL (UNII: L7T10EIP3A)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PPG-9 (UNII: I29VQH0G0B)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1357-1	355 mL in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	08/02/2009

Labeler - Conopco Inc. d/b/a Unilever (001375088)

Establishment
Name	Address	ID/FEI	Business Operations
Unilever Supply Chain Co. d/b/a Unilever		043510056	manufacture(64942-1357)