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Genrx anti-bacterial gel - Medication Information

Product NDC Code 59088-299
Drug Name

Genrx anti-bacterial gel

Type Brand
Active Ingredients
Alcohol 62 ml/100ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 581660
Application Number M014
Labeler Name PureTek Corporation
Packages
Package NDC Code Description
59088-299-08 118 ml in 1 bottle, pump (59088-299-08)
59088-299-31 500 ml in 1 bottle, dispensing (59088-299-31)
59088-299-39 710 ml in 1 bottle, pump (59088-299-39)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Alcohol 62% (v/v)

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 ■ Dispense and rub onto hands until dry. Do not rinse off. ■ Children under 6 years of age should use this product under supervision.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Aloe Barbadensis (aloe vera) Leaf Juice, Aminomethyl Propanol, Butyrospermum Parkii (Shea) Butter, Carbomer, Glycerin, Isopropyl Myristate, Water (Aqua)

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 Hand sanitizer to help reduce bacteria on the skin

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
GenRx Anti-Bacterial Gel Alcohol SHEA BUTTER AMINOMETHYL PROPANEDIOL ALOE VERA LEAF GLYCERIN CARBOMER HOMOPOLYMER TYPE C ISOPROPYL MYRISTATE PANTHENOL WATER ALCOHOL ALCOHOL

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.
GenRx Hand Sanitizing Gel (24 fl oz) Label

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.
Other information ■ Do not store above 110°F (43°C)

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

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 If irritation or rash appears and lasts.

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 or near 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 Flammable. Keep away from fire or flame.

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