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Gold antibacterial hand - Medication Information

Product NDC Code 76176-064
Drug Name

Gold antibacterial hand

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1046593
Application Number part333A
Labeler Name NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Packages
Package NDC Code Description
76176-064-01 473 ml in 1 bottle, pump (76176-064-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active ingredient Benzalkonium Chloride 0.13 percent

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 wet hands as needed lather vigorously for at least 15 seconds rinse and dry thoroughly

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients: Water (Aqua), Cocamidopropye Betaine, PEG-6000 Distearate, Sodium Cocoamphoacetate, Fragrance, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No.5, D&C Red No.33

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 for hand washing to decrease bacteria on the skin.

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.
GOLD ANTIBACTERIAL HAND BENZALKONIUM CHLORIDE WATER COCAMIDOPROPYL BETAINE SODIUM COCOAMPHOACETATE IODOPROPYNYL BUTYLCARBAMATE CITRIC ACID MONOHYDRATE METHYLISOTHIAZOLINONE BENZALKONIUM CHLORIDE BENZALKONIUM D&C RED NO. 33 FD&C YELLOW NO. 5

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

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.

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 and redness develops.

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 avoid contact with eyes. In case of eye contact, flush with water.

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