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Antiperspirant dry 1.6 oz men antiperspirant - Medication Information

Product NDC Code 57337-109
Drug Name

Antiperspirant dry 1.6 oz men antiperspirant

Type Brand
Active Ingredients
Aluminum chlorohydrate 23.3 g/100g
Route TOPICAL
Dosage Form AEROSOL, SPRAY
Application Number M019
Labeler Name Rejoice International Inc
Packages
Package NDC Code Description
57337-109-01 45 g in 1 bottle, spray (57337-109-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient ........................................................................... Purpose Aluminum Chlorohydrate 23.3% .................................................. Antiperspirant

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions For underarm use only. Shake can well before each use. Hold can 6 inches away from skin. Spray underarm and spray

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
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

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Reduces underarm wetness

Purpose

Information about the drug product’s indications for use.
Antiperspirant

Spl product data elements

Usually a list of ingredients in a drug product.
Antiperspirant Dry 1.6 oz Men Antiperspirant Aluminum Chlorohydrate PPG-14 BUTYL ETHER ALKYL (C12-15) BENZOATE PROPANE BENTONITE 1,1-DIFLUOROETHANE CYCLOMETHICONE 5 ALCOHOL BUTYLATED HYDROXYTOLUENE DISTEARDIMONIUM HECTORITE .ALPHA.-TOCOPHEROL ACETATE SUNFLOWER OIL BUTANE ISOPROPYL MYRISTATE ALUMINUM STARCH OCTENYLSUCCINATE DIMETHICONE ALUMINUM CHLOROHYDRATE ALUMINUM CHLOROHYDRATE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Label

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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 o F/50 o C 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

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API