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Purell antimicrobial fragrance free foaming hand sp - Medication Information

Product NDC Code 21749-114
Drug Name

Purell antimicrobial fragrance free foaming hand sp

Type Brand
Active Ingredients
Benzalkonium chloride .13 mg/100ml
Route TOPICAL
Dosage Form LIQUID
Application Number 505G(a)(3)
Labeler Name GOJO Industries, Inc.
Packages
Package NDC Code Description
21749-114-40 1200 ml in 1 package (21749-114-40)
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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.
Directions • Wet hands • Apply a small amount of soap and work into a rich lather • Rinse thoroughly with potable water • Dry hands completely

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water (Aqua), Propanediol, Glycerin, Cocamidopropyl Betaine, PEG-80 Sorbitan Laurate, Citric Acid, Ethylhexylglycerin, Lauramine Oxide, Polyquaternium-10, Trisodium Ethylenediamine Disuccinate, Phenoxyethanol

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 • Handwash to help decrease bacteria on the skin • Recommended for repeated use

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
PURELL Antimicrobial Fragrance Free Foaming Hand SP Benzalkonium Chloride Benzalkonium Chloride BENZALKONIUM Water PROPANEDIOL Glycerin Cocamidopropyl Betaine PEG-80 Sorbitan Laurate CITRIC ACID MONOHYDRATE Ethylhexylglycerin Lauramine Oxide POLYQUATERNIUM-10 (10000 MPA.S AT 2%) TRISODIUM ETHYLENEDIAMINE DISUCCINATE PHENOXYETHANOL

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.
Product 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 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 rash appears and lasts

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 do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

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 When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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