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Coralite antibacterial moist - Medication Information

Product NDC Code 65923-831
Drug Name

Coralite antibacterial moist

Type Brand
Active Ingredients
Benzalkonium chloride .115 g/1
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1049374
Application Number M003
Labeler Name United Exchange Corp.
Packages
Package NDC Code Description
65923-831-30 30 solution in 1 pouch (65923-831-30)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active Ingredient Purpose Benzalkonium Chloride 0.115%............................................................ Antibacterial

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.
Distributed by: UNITED EXCHANGE CORP. 17211 Valley View Ave. Cerritos, CA 90703 MADE IN CHINA

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients aqua, aloe barbadensis leaf juice powder, 2-Bromo-2-Nitropropane-1,3-Diol, Chamomilla Recutita Flower Extract, Citric Acid, Iodopropynl butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Sodium Citrate, Terasodium EDTA

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.
Directions adults and children 12 years and over Rub on hands for 30 seconds and allow skin to dry without wiping children under 2 years ask a doctor before use
adults and children 12 years and overRub on hands for 30 seconds and allow skin to dry without wiping
children under 2 yearsask a doctor before use

Purpose

Information about the drug product’s indications for use.
Uses Decreases bacteria on skin and surfaces

Spl product data elements

Usually a list of ingredients in a drug product.
Coralite Antibacterial Moist Benzalkonium Chloride ALOE VERA LEAF BRONOPOL CITRIC ACID ACETATE LAURYL GLUCOSIDE PHENOXYETHANOL POLYSORBATE 20 PROPYLENE GLYCOL SODIUM CITRATE EDETATE SODIUM BENZALKONIUM CHLORIDE BENZALKONIUM WATER MATRICARIA CHAMOMILLA ROOT

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.
83103

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 Poision Control Center right away.

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 rash develops and persists for more than 72 hours.

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 this product avoid contact with the eyes, if contact occurs rinse 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.
Warnings 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