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Firstar alcohol prep pad - Medication Information

Product NDC Code 71734-112
Drug Name

Firstar alcohol prep pad

Type Brand
Active Ingredients
Isopropyl alcohol 70 g/100g
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 797544
Application Number M003
Labeler Name JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Packages
Package NDC Code Description
71734-112-01 .4 g in 1 pouch (71734-112-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Isopropyl 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.
Directions Apply topically as needed to cleanse intended area and discard after single use. Other Information: Store at room temperature.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Purified 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.
Uses: For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.

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.
FIRSTAR Alcohol Prep Pad Isopropyl Alcohol Isopropyl Alcohol ISOPROPYL ALCOHOL water

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.
Principal Display Panel

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

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
For external use only. Flammable. Keep away from fire or flame. Do not use with electrocautery procedures; in the eyes. If contact accurs ,flush eyes with water. Stop use if irritation and redness develop. If condition persists consult your health care practioner.

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.

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. Do not use with electrocautery procedures; in the eyes. If contact accurs ,flush eyes with water. Stop use if irritation and redness develop. If condition persists consult your health care practioner. Keep out of reach of children. 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