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Product NDC Code | 64942-1447 | ||||
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Drug Name | Degree motionsense stress control dry antiperspirant |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | AEROSOL, SPRAY | ||||
Application Number | part350 | ||||
Labeler Name | Conopco, Inc. d/b/a/ Unilever | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient Aluminum Chlorohydrate (23.3%)
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.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.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.
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.Uses reduces underarm wetness
Purpose
Information about the drug product’s indications for use.Purpose antiperspirant
Spl product data elements
Usually a list of ingredients in a drug product.Degree MotionSense Stress Control Dry Antiperspirant Aluminum Chlorohydrate BUTANE CYCLOMETHICONE 5 1,1-DIFLUOROETHANE ISOBUTANE PPG-14 BUTYL ETHER DISTEARDIMONIUM HECTORITE PROPANE BUTYLATED HYDROXYTOLUENE MEDIUM-CHAIN TRIGLYCERIDES PROPYLENE CARBONATE MALTODEXTRIN HYDRATED SILICA STARCH, CORN SILICON DIOXIDE CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM SODIUM BENZOATE 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.Packaging image description
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Drug Facts
48 HR antiperspirant GOES ON INSTANTLY DRY
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
Questions
A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.Questions? Call toll-free 1-866-334-7331
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 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 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
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