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
- 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 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)
