Label: DEGREE EXTREME ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray
- NDC Code(s): 64942-1381-1
- 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 28, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
WARNINGS:
• 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
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients: Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Caprylic/Capric Triglyceride, Sodium Starch Octenylsuccinate, Propylene Carbonate, Maltodextrin, Hydrated Silica, Hydrolyzed Corn Starch, Gelatin Crosspolymer, Silica, Cellulose Gum, Sodium Benzoate.
- QUESTIONS
- Packaging
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INGREDIENTS AND APPEARANCE
DEGREE EXTREME ANTIPERSPIRANT
aluminum chlorohydrate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1381 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) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0) ISOBUTANE (UNII: BXR49TP611) PPG-14 BUTYL ETHER (UNII: R199TJT95T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) PROPANE (UNII: T75W9911L6) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PROPYLENE CARBONATE (UNII: 8D08K3S51E) MALTODEXTRIN (UNII: 7CVR7L4A2D) HYDRATED SILICA (UNII: Y6O7T4G8P9) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1381-1 107 g in 1 CAN; Type 0: Not a Combination Product 11/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 11/01/2014 Labeler - Conopco Inc. d/b/a Unilever (001375088)
