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E2 hand sanitizer - Medication Information

Product NDC Code 64542-017
Drug Name

E2 hand sanitizer

Type Generic
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1046593
Application Number part333A
Labeler Name State Industrial Products
Packages
Package NDC Code Description
64542-017-03 208197 ml in 1 drum (64542-017-03)
64542-017-09 3785 ml in 1 bottle (64542-017-09)
64542-017-41 1000 ml in 1 bag (64542-017-41)
64542-017-46 675 ml in 1 bottle, pump (64542-017-46)
64542-017-94 3000 ml in 1 bottle (64542-017-94)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient 0.13% Benzalkonium Chloride

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 To decrease bacteria on skin, apply a small amount covering hands with product for 30 seconds. Add water, lather and rinse.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocammidopropyl Betaine, PEG-6 Cocamide, Hydroxyethylcellulose, Laurtrimonium Chloride, Iodopropynl Butylcarbamate, Methylisothiazolinone

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 For handwashing to decrease bacteria on skin.

Purpose

Information about the drug product’s indications for use.
Purpose Antibacterial Agent

Spl product data elements

Usually a list of ingredients in a drug product.
E2 Hand Sanitizer E2 Hand Sanitizer COCAMIDOPROPYL BETAINE LAURTRIMONIUM CHLORIDE METHYLISOTHIAZOLINONE CETYL HYDROXYETHYLCELLULOSE (350000 MW) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PEG-6 COCAMIDE IODOPROPYNYL BUTYLCARBAMATE BENZALKONIUM CHLORIDE BENZALKONIUM WATER

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.
State 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, contact a physician or poison control center.

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. Avoid contact with eyes. If contact occurs, flush with water. Stop use and ask a doctor if, in rare instances, redness or irritation develops and persists for more than 72 hours.

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