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Foaming hand sanitizer - Medication Information

Product NDC Code 51706-940
Drug Name

Foaming hand sanitizer

Type Brand
Active Ingredients
Benzalkonium chloride .1 g/100g
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1038799
Application Number part333A
Labeler Name Landy International
Packages
Package NDC Code Description
51706-940-01 51 g in 1 bottle (51706-940-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient(s) Benzalkonium Chloride 0.1%

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 Dispense a palm-sized amount onto hands·Rub hands together until dry

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water (Aqua),PEG-40 Hydrogenated Castor Oil, Glycerin, Fragrance (ParfumDidecyldimonium Chloride, Phenoxy- ethanol, Polyaminopropyl Biguanide, Citric Acid, Citrus Limon (lemon)Peel Oil, Yellow 5(Cl19140), Red 4 (CI 14700) Eucalyptus Globulus Leaf Oil,Blue 1(CI 42090) Vanilla Planifolia Fruit Oil,Red 33(CI 172000) Mangifera Indica(mango)Seed Oil

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.
Use Decreases bacteria on hands.

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.
Foaming Hand Sanitizer Benzalkonium chloride POLYOXYL 40 HYDROGENATED CASTOR OIL POLYAMINOPROPYL BIGUANIDE CITRIC ACID MONOHYDRATE EUCALYPTUS OIL FD&C RED NO. 4 MANGO SEED OIL VANILLA PLANIFOLIA OIL PHENOXYETHANOL GLYCERIN WATER BENZALKONIUM CHLORIDE BENZALKONIUM DIDECYLDIMONIUM CHLORIDE FD&C BLUE NO. 1 FD&C YELLOW NO. 5 LEMON OIL D&C RED NO. 33

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 - Principal Display Panel 1 2 3 4

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, except under adult supervision. 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 Use only directed. For external use only. When using this product avoid contact with eyes. lf contact occurs, rinse thoroughly with water. Stop use and ask doctor if irritation and redness develop or increase.

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