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Fa hand sanitizer gel 70% (ethanol) - Medication Information

Product NDC Code 74932-100
Drug Name

Fa hand sanitizer gel 70% (ethanol)

Type Brand
Active Ingredients
Alcohol 70 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581662
Application Number M003
Labeler Name HLB CO.,LTD_Healthcare
Packages
Package NDC Code Description
74932-100-01 1 tube in 1 box (74932-100-01) / 57 ml in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Ethyl Alcohol 70%

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.
Use Hand Sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Carbormer, Fragrance, Glycerin, Triethanolamine, Water.

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 Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

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.
FA Hand Sanitizer Gel 70% (Ethanol) Hand Sanitizer CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE WATER TROLAMINE ALCOHOL ALCOHOL GLYCERIN

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 LABEL.PRINCIPAL DISPLAY PANEL Image of carton

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 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 useing this product -do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. -avoid contact with broken skin. -do not inhale or ingest.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store below 86 o F (Between 1 o C-30 o C). May discolor certain fabrics or surfaces.

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 - hands Flammable, Keep awa 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