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Hand sanitizer - Medication Information

Product NDC Code 78495-169
Drug Name

Hand sanitizer

Type Brand
Active Ingredients
Alcohol 70 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581662
Application Number part333E
Labeler Name Ultra Distributors Inc.
Packages
Package NDC Code Description
78495-169-01 500 ml in 1 bottle, pump (78495-169-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Ethyl Alcohol 70%

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 wet hands thoroughly with product and allow to dry without wiping. for children under 6 , use only under adult supervision. not recommented for infants .

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients acrylates/C10-C30 alkyl acrylate crosspolymer,aloe barbadensis leaf juice, aminomethyl propanol, glycerin, maltodextrin, propylene glycol, water , tocopheryl acetate

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 to decrease 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.
Hand Sanitizer ETHYL ALCOHOL MALTODEXTRIN PROPYLENE GLYCOL WATER ALOE VERA LEAF GLYCERIN CARBOMER INTERPOLYMER TYPE A (55000 CPS) .ALPHA.-TOCOPHEROL ACETATE ALCOHOL ALCOHOL AMINOMETHYLPROPANOL

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.
image of bottle 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(1-800-222-1222)right away .

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if . irritation or redness develops. condition persists for more than 72 hours

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin. do not inhale or ingest.

Storage and handling

Information about safe storage and handling of the drug product.
Other information do not store above 105°F may discolor some fabics harmful to wood finished and plastics

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: hands 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