Label: ANTIPERSPIRANT DRY 1.6 OZ MEN ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray
- NDC Code(s): 57337-109-01
- Packager: Rejoice International Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 28, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only.
Flammable. Do not use while smoking or near heat or 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 oF/50 oC or in enclosed places that could overheat.
- Do not use on broken skin.
- Ask a doctor before using, if you have kidney disease
- When using this product.
- Keep away from face and mouth to avoid breathing it
- avoid spraying in eyes
- USE ONLY AS DIRECTED. INTENTIONAL MISSUSE BY DELIBERATELY CONCENTRATING AND INHAILING THE CONTENTS CAN BE HARMFUL OR FATAL.
- Stop use if rash or irritation occurs
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients
Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Alcohol, PPG-14 Butyl Ether, Helianthus Annuus Seed Oil, Isopropryl Myristate, C12-15 Alkyl Benzoate, Frangrance, Propane, Aluminum Starch Ocetenylsuccinate, Disteardimonium Hectorite, Dimethicone, Tocopheryl Acetate, BHT, Bentonite, Lauryl Phosphate
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIPERSPIRANT DRY 1.6 OZ MEN ANTIPERSPIRANT
aluminum chlorohydrate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57337-109 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 PPG-14 BUTYL ETHER (UNII: R199TJT95T) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) PROPANE (UNII: T75W9911L6) BENTONITE (UNII: A3N5ZCN45C) 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALCOHOL (UNII: 3K9958V90M) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SUNFLOWER OIL (UNII: 3W1JG795YI) BUTANE (UNII: 6LV4FOR43R) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) DIMETHICONE (UNII: 92RU3N3Y1O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57337-109-01 45 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M019 01/13/2020 Labeler - Rejoice International Inc (078741245) Establishment Name Address ID/FEI Business Operations BLUE SEA AEROSOL & DAILY CARE CO., LTD. 544373091 manufacture(57337-109)
