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Antibacterial hand lavender sage - Medication Information

Product NDC Code 78784-003
Drug Name

Antibacterial hand lavender sage

Type Brand
Active Ingredients
Benzalkonium chloride 1.3 mg/ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1046593
Application Number part333E
Labeler Name GUANGZHOU SLUJ SPECIAL CHEMICAL CO., LTD
Packages
Package NDC Code Description
78784-003-01 500 ml in 1 bottle (78784-003-01)
78784-003-02 3780 ml in 1 bottle (78784-003-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient 0.13% Benalkonium chloride Purpose 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.
Directions Wash hands and rinse

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water(Aqua),Sodium Laureth Sulfate,Cocamidopropyl Betaine, Sodium Chloride, Sodium Benzoate Phenoxyethanol,Polysorbate 20, Fragrance, Glycerin

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 helps eliminate bacteria on hands

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Antibacterial Hand Lavender Sage BENZALKONIUM CHLORIDE WATER SODIUM LAURETH SULFATE COCAMIDOPROPYL BETAINE SODIUM CHLORIDE SODIUM BENZOATE PHENOXYETHANOL POLYSORBATE 20 GLYCERIN BENZALKONIUM CHLORIDE BENZALKONIUM

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 Labeling:500ml Label Package Labeling:3.78L Label2

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts

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 the reach of children, except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

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 do not use in near the eyes. In case of contact, rinse eyes throughly 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 When using this product do not use in near the eyes. In case of contact, rinse eyes throughly with water. Keep out of the reach of children, except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

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