Label: AXE FREEZE ANTIDANDRUFF- pyrithione zinc shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1357-1 - Packager: Conopco Inc. d/b/a Unilever
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 24, 2014
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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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
- 12 FL OZ PDP
- 12 FL OZ back
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INGREDIENTS AND APPEARANCE
AXE FREEZE ANTIDANDRUFF
pyrithione zinc shampooProduct 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)