Label: DEGREE- motionsense ultraclear black and white dry spray antiperspirant aerosol, spray
- NDC Code(s): 64942-1568-1
- Packager: Conopco Inc. d/b/a Unilever
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 28, 2020
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- DEGREE MOTIONSENSE ULTRACLEAR BLACK AND WHITE DRY SPRAY ANTIPERSPIRANT - aluminum chlorohydrate aerosol, spray
- Drug Facts
- Purpose:
- Uses
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Warnings
• FLAMMABLE UNTILFULLY DRY. 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 - Directions
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Inactive ingredients
Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Disteardimonium Hectorite, Propane, Fragrance (Parfum), BHT, Propylene Carbonate, Caprylic/Capric Triglyceride, Sodium Starch Octenylsuccinate, Maltodextrin, Hydrated Silica, Hydrolyzed Corn Starch, Gelatin Crosspolymer, Silica, Cellulose Gum, Sodium Benzoate, Alpha-Isomethyl Lonone, Benzyl Alcohol, Benzyl Salicylate, Butylphenyl Methylpropional, Citronellol, Hexyl Cinnamal, Hydroxycitronellal, Limonene, Linalool.
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INGREDIENTS AND APPEARANCE
DEGREE
motionsense ultraclear black and white dry spray antiperspirant aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1568 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 LINALOOL, (+/-)- (UNII: D81QY6I88E) MALTODEXTRIN (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) SODIUM BENZOATE (UNII: OJ245FE5EU) BENZYL ALCOHOL (UNII: LKG8494WBH) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) BENZYL SALICYLATE (UNII: WAO5MNK9TU) BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) LIMONENE, (+)- (UNII: GFD7C86Q1W) BUTANE (UNII: 6LV4FOR43R) 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ISOBUTANE (UNII: BXR49TP611) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) PROPANE (UNII: T75W9911L6) PROPYLENE CARBONATE (UNII: 8D08K3S51E) HYDRATED SILICA (UNII: Y6O7T4G8P9) STARCH, CORN (UNII: O8232NY3SJ) PPG-14 BUTYL ETHER (UNII: R199TJT95T) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1568-1 28 g in 1 CAN; Type 0: Not a Combination Product 01/31/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 01/31/2018 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(64942-1568)