Label: AXE- gold dry spray antiperspirant aerosol, spray
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1511-1 - 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 September 11, 2017
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- Official Label (Printer Friendly)
- AXE GOLD DRY SPRAY ANTIPERSPIRANT - aluminum chlorohydrate aerosol, spray
- Drug Facts
- Purpose
- Uses
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Warnings
• For external use only
• FLAMMABLE. DO NOT USE NEAR HEAT, FLAME, OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH
• Keep away from face and mouth to avoid breathing in.
• Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F/50°C or in enclosed places that could overheat
• Do not use on broken skin. Stop use if rash or irritation occurs.
• Ask a doctor before using if you have kidney disease.
• USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.
Help stop inhalation abuse. For information visit www.inhalant.org - KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
AXE
gold dry spray antiperspirant aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1511 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 20.2 g in 100 g Inactive Ingredients Ingredient Name Strength BUTANE (UNII: 6LV4FOR43R) 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ISOBUTANE (UNII: BXR49TP611) PPG-14 BUTYL ETHER (UNII: R199TJT95T) PROPANE (UNII: T75W9911L6) PROPYLENE CARBONATE (UNII: 8D08K3S51E) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1511-1 107 g in 1 CAN; Type 0: Not a Combination Product 09/11/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 09/11/2017 Labeler - Conopco Inc. d/b/a/ Unilever (001375088)