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Luxury antibacterial foaming handsoap - Medication Information

Product NDC Code 56131-859
Drug Name

Luxury antibacterial foaming handsoap

Type Brand
Active Ingredients
Benzalkonium chloride 1.3 mg/100ml
Route TOPICAL
Dosage Form LIQUID
Application Number 505G(a)(3)
Labeler Name RD Food Service DBA Restaurant Depot
Packages
Package NDC Code Description
56131-859-29 1000 ml in 1 bag (56131-859-29)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
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.
Place enough product on your palm and scrub hands thoroughly over both surfaces of both hands. Rinse with clean water

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Water, Phenoxyethanol, cocamine oxide, caprylyl/capryl glucoside, Porpylene glycol, PEG-4 rapeseedamide,cocamidopropyl hydroxysultaine, glycerin, fragrance, tetrasodium EDTA, Citric Acid, Acid Blue 9

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.
Antibacterial Hand Cleaner Use in daycare centers, hospitals, nursing homes, physicians offices, dental offices and clinics

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Luxury Antibacterial Foaming HandSoap Benzalkonium chloride N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) .BETA.-CITRONELLOL, (+/-)- GLYCERIN COCAMINE OXIDE SODIUM CHLORIDE LIME OIL COCAMIDOPROPYL HYDROXYSULTAINE SODIUM HYDROXIDE CITRAL PHENOXYETHANOL SODIUM GLYCOLATE BENZALKONIUM CHLORIDE BENZALKONIUM EDETATE SODIUM ALCOHOL FD&C BLUE NO. 1 LINALOOL TRISODIUM NITRILOTRIACETATE ANHYDROUS CITRIC ACID METHYL DIHYDROJASMONATE (SYNTHETIC) METHYLCHLOROISOTHIAZOLINONE PEG-4 RAPESEEDAMIDE PROPYLENE GLYCOL 2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE CAPRYLYL/CAPRYL GLUCOSIDE MAGNESIUM NITRATE 2-METHYLUNDECANAL METHYLISOTHIAZOLINONE BENZYL ACETATE GERANIOL ALLYL CYCLOHEXANEPROPIONATE GERANYL ACETATE CITRONELLYL ACETATE 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.
label

Instructions for use

Information about safe handling and use of the drug product.
Read entire label before using this product place enough product on your palm and scrub thoroughly over all surfaces of both hands. Rinse with clean water.

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 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.
For external use only. Do not ingest When using this product avoud contact with eyes disocntinue use if irritation or redness develops I irritation persist for more than 72 hours, consult a physicain

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