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Zoono alcohol free hand sanitizer - Medication Information

Product NDC Code 69221-601
Drug Name

Zoono alcohol free hand sanitizer

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1049254
Application Number 505G(a)(3)
Labeler Name Zoono Holdings USA LLC
Packages
Package NDC Code Description
69221-601-11 50 ml in 1 bottle (69221-601-11)
69221-601-13 150 ml in 1 bottle (69221-601-13)
69221-601-14 500 ml in 1 bottle (69221-601-14)
69221-601-15 1000 ml in 1 bottle (69221-601-15)
69221-601-16 3785 ml in 1 bottle (69221-601-16)
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Active ingredient

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

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.
Uses For personal hand sanitizing and to reduce bacteria on the skin. Recommended for repeated use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Fragrances, Silica Complex 3-(Trimethoxysilyl) Propyl Dimethyl Octadecyl Ammonium Chloride, 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.
Directions Apply liberally to the hands and gently rub until dry.

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.
Zoono Alcohol Free Hand Sanitizer benzalkonium chloride 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.
typical

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.
Stop use and ask a doctor if irritation and redness develop

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 childres Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? Telephone" 1-844-966-6687 Monday through Friday 8:00am til 5:00pm EST

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. Do not use in the eyes. When using this product avoid contact with eyes. In case of eye contact flush eyes with water.

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