Label: AXE DRY PHOENIX- aluminum zirconium tetrachlorohydrex gly stick
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1164-6, 64942-1164-8 - Packager: Conopco Inc. d/b/a Unilever
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 November 15, 2022
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- ACTIVE INGREDIENT
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- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
AXE DRY PHOENIX
aluminum zirconium tetrachlorohydrex gly stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1164 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 18.2 g in 100 g Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PPG-14 BUTYL ETHER (UNII: R199TJT95T) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) TALC (UNII: 7SEV7J4R1U) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1164-6 48 g in 1 CONTAINER; Type 0: Not a Combination Product 06/01/2011 2 NDC:64942-1164-8 14 g in 1 CONTAINER; Type 0: Not a Combination Product 06/01/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 06/01/2011 Labeler - Conopco Inc. d/b/a Unilever (001375088)