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Product NDC Code | 56131-859 | ||||
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Drug Name | Luxury antibacterial foaming handsoap |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | LIQUID | ||||
Application Number | 505G(a)(3) | ||||
Labeler Name | RD Food Service DBA Restaurant Depot | ||||
Packages |
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Check if available Online | Get Medication Prices online with Discount |
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