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Hand sanitizer - Medication Information

Product NDC Code 64542-207
Drug Name

Hand sanitizer

Type Generic
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1020365
Application Number part333A
Labeler Name State Industrial Products
Packages
Package NDC Code Description
64542-207-17 50 ml in 1 bottle (64542-207-17)
64542-207-41 1000 ml in 1 bag (64542-207-41)
64542-207-46 500 ml in 1 bottle (64542-207-46)
64542-207-91 547 ml in 1 bottle (64542-207-91)
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Active ingredient

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

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 Apply a small amount to palm. Briskly rub, covering hands with product until dry.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water, Propylene Glycol, Fragrance, Tocopheryl Acetate, Tetrasodium EDTA, Cocamidoprpyl Betaine, PEG-7 Glyceryl Cocoate, Phenoxyethanol, Aloe Barbadensis Leaf Juice

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 Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

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.
Hand Sanitizer Hand Sanitizer DITETRACYCLINE TETRASODIUM EDETATE PROPYLENE GLYCOL 1-MYRISTATE .ALPHA.-TOCOPHEROL ACETATE, D- PEG-7 GLYCERYL COCOATE ALOE VERA LEAF PHENOXYETHANOL BENZALKONIUM CHLORIDE BENZALKONIUM WATER COCAMIDOPROPYL BETAINE

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 Gentle Fresh

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, if in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.

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