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Product NDC Code | 50157-503 | ||||||||||||
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Drug Name | Germs be gone hand sanitizer |
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Type | Brand | ||||||||||||
Active Ingredients |
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Route | TOPICAL | ||||||||||||
Dosage Form | GEL | ||||||||||||
RxCUI drug identifier | 1041498 | ||||||||||||
Application Number | part333E | ||||||||||||
Labeler Name | Brands International | ||||||||||||
Packages |
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Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredients Ethyl Alcohol 80% w/w Purpose: Antiseptic
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 Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when using this product.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients water, isopropyl alcohol, glycerin, carbomer, aminomethyl propanol, fragrance, propylene glycol, Aloe, Tocopheryl Acetate. isopropyl myristate
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 helps reduce bacteria on the skin that could cause disease Recommended for repeated use
Purpose
Information about the drug product’s indications for use.Purpose Antiseptic
Spl product data elements
Usually a list of ingredients in a drug product.Germs Be Gone Hand Sanitizer Ethyl Alcohol WATER ISOPROPYL ALCOHOL ISOPROPYL MYRISTATE ALOE VERA LEAF PROPYLENE GLYCOL GLYCERIN CARBOMER COPOLYMER TYPE A .ALPHA.-TOCOPHEROL ACETATE, D- AMINOMETHYLPROPANOL ALCOHOL ALCOHOL
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.NDC: 50157-503-01: 118ml 50157-503-02: 148ml 50157-503-05: 148ml : Bottle, Spray 50157-503-03: 236ml 50157-503-04: 443ml IMG_1688 14oz 4oz 5oz 8oz
Ask doctor
Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.Ask Doctor Stop Use and Ask a doctor if irritation or redness develops
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 Poison Control right away
Other safety information
Information about safe use and handling of the product that may not have been specified in another field.Safety Instructions Flammable, Keep away from fire and flame
Other Information Store below 110°F (43°C) May discolor certain fabrics or surfaces.
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. Keep away from fire or flame.
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