![AXE ADRENALINE ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO INC. D/B/A UNILEVER]](https://medic.hrt.org//dailymed/images/b6516ac0-00c5-4aaf-a2f9-de92921c0319/AxeAdrenalineDrySprayAPPDP.jpg)
| NDC | 64942-1407-1, 64942-1407-2 |
| Set ID | b6516ac0-00c5-4aaf-a2f9-de92921c0319 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | Conopco Inc. d/b/a Unilever |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART350 |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
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 degrees F/50 degrees 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 - DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- 3.8 oz PDP
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INGREDIENTS AND APPEARANCE
AXE ADRENALINE ANTIPERSPIRANT
aluminum chlorohydrate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1407 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 23.3 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) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) PROPANE (UNII: T75W9911L6) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PROPYLENE CARBONATE (UNII: 8D08K3S51E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1407-1 107 g in 1 CAN; Type 0: Not a Combination Product 12/01/2015 2 NDC:64942-1407-2 28 g in 1 CAN; Type 0: Not a Combination Product 12/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 12/01/2015 Labeler - Conopco Inc. d/b/a Unilever (001375088) Establishment Name Address ID/FEI Business Operations Unilever Manufacturera, S. de R.L. de C.V. 812625061 manufacture(64942-1407)
