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Pfa - Medication Information

Product NDC Code 75742-008
Drug Name

Pfa

Type Brand
Active Ingredients
Alcohol 70 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581662
Application Number part333A
Labeler Name Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Packages
Package NDC Code Description
75742-008-01 2 ml in 1 pouch (75742-008-01)
75742-008-02 237 ml in 1 bottle, pump (75742-008-02)
75742-008-03 375 ml in 1 bottle, pump (75742-008-03)
75742-008-04 500 ml in 1 bottle, pump (75742-008-04)
75742-008-05 60 ml in 1 bottle, plastic (75742-008-05)
75742-008-06 80 ml in 1 bottle, plastic (75742-008-06)
75742-008-07 100 ml in 1 bottle, plastic (75742-008-07)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Ethyl Alcohol 70% 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 Place enough product on hands to cover hands & rub together briskly until the liquid is dry. Children under 6 should be supervised when using Sanitizers.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Carbomer, Glycerin, Grapefruit seed extract, Mentha Oil, Propylene Glycol, Purified water, Sophora extract, Triethanolamine

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 Hand sanitizing to help reduce bacteria on the skin.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
PFA ETHYL ALCOHOL CITRUS PARADISI SEED MENTHA ARVENSIS LEAF OIL TROLAMINE GLYCERIN WATER ALCOHOL ALCOHOL CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE PROPYLENE GLYCOL SOPHORA FLAVESCENS 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.
Package Label - Principal Display Panel 60 mL/2 fl.oz Principal Display Panel

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 immediately.

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 or persists.

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. In case of contact, flush eyes thoroughly with water.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store below 110F (43C) 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. 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