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Moonlite antibacterial - Medication Information

Product NDC Code 50157-511
Drug Name

Moonlite antibacterial

Type Brand
Active Ingredients
Benzalkonium chloride 1.3 mg/ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1046593
Application Number part333A
Labeler Name Brands International Corporation
Packages
Package NDC Code Description
50157-511-23 236 ml in 1 bottle, plastic (50157-511-23)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
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.
Direction Adults and children over 2 year For occasional and personal domestic use Supervise children when use this product Lather in hands with water for at least 30 seconds Rinse well

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Water,Lauramidopropylamine Oxide ( Triaminox LO ), Lauryl Glucoside, Citric Acid, PEG-150 distearate, Glycol Stearate, PEG-7 Glyceryl Cocoate,Cetrimonium Chloride, Tetrasodium EDTA,Isopropyl myristate, Aloe Leaf, Tocopheryl Acetate, Methylchloroisothiazolinone, Methylisothiazolinone,

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 Effective in destorying(harmful) bacteria to provide antiseptic cleansing.

Purpose

Information about the drug product’s indications for use.
Purpose - Antiseptique(skin)cleanser

Spl product data elements

Usually a list of ingredients in a drug product.
Moonlite Antibacterial Benzalkonium Chloride LAURAMIDOPROPYLAMINE OXIDE LAURYL GLUCOSIDE PEG-150 DISTEARATE GLYCOL STEARATE WATER PEG-7 GLYCERYL COCOATE CITRIC ACID MONOHYDRATE CETRIMONIUM CHLORIDE EDETATE SODIUM ISOPROPYL MYRISTATE ALOE VERA LEAF METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE BENZALKONIUM CHLORIDE BENZALKONIUM .ALPHA.-TOCOPHEROL ACETATE

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.
1

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

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
S tore below 110F(43) May discolor certain fabrics or surfaces.

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 redness develops

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 the product avoid contact wiith eyes. If contact occurs rinse eye 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.
Warning For external use only

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