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Advanced alcohol foaming hand sanitizer - Medication Information

Product NDC Code 65601-802
Drug Name

Advanced alcohol foaming hand sanitizer

Type Brand
Active Ingredients
Alcohol .6787 ml/ml
Route TOPICAL
Dosage Form LIQUID
Application Number 505G(a)(3)
Labeler Name Betco Corporation LLC
Packages
Package NDC Code Description
65601-802-04 3785 ml in 1 bottle, plastic (65601-802-04)
65601-802-29 1000 ml in 1 bag (65601-802-29)
65601-802-55 208175 ml in 1 drum (65601-802-55)
65601-802-88 500 ml in 1 bottle, plastic (65601-802-88)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Ethjyl Alcohol

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.
dosage Please read entire label before using thsi product. Place enough product on your palm to tnoroughly cover your hands, Rub hands together briskyl until dry.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
inactives Aloe Barbadensis Leaf Juice, D&C Green #5, PEG 10 Perfluorohexylethyl acrylate copolymer, Perluorohexylethyl alcohol, propylene glycol, water

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.
usage Hand sanitizer to reduce mocroorganisms on the skin.. Use this product when soap and water are not available.

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.
Advanced Alcohol Foaming Hand Sanitizer Ethyl Alcohol WATER PROPYLENE GLYCOL ALCOHOL ALCOHOL D&C GREEN NO. 5 ALOE VERA LEAF PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER 2-(PERFLUOROHEXYL)ETHANETHIOL

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.
package label product label package 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 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. This product contains ethyl alcohol. Keep away from heat or flame. When using this product avoid contact with eyes. If contact occurs rinse thoroughly with water. Stop use and ask a doctor if irritation or rash 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