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First aid only alcohol antiseptic pad - Medication Information

Product NDC Code 0924-0009
Drug Name

First aid only alcohol antiseptic pad

Type Brand
Active Ingredients
Isopropyl alcohol 70 g/100g
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 797544
Application Number part333A
Labeler Name Acme United Corporation
Packages
Package NDC Code Description
0924-0009-00 1 g in 1 packet (0924-0009-00)
0924-0009-01 100 packet in 1 carton (0924-0009-01) / 1 g in 1 packet
0924-0009-02 200 packet in 1 carton (0924-0009-02) / 1 g in 1 packet
0924-0009-03 10 packet in 1 carton (0924-0009-03) / 1 g in 1 packet
0924-0009-04 20 packet in 1 carton (0924-0009-04) / 1 g in 1 packet
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Active Ingredients 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 Directions •Wipe Injection site vigorously and discard.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients 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 Uses •For preparation of the skin prior to injection

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
First Aid Only Alcohol Antiseptic Pad Alcohol Pad WATER ISOPROPYL ALCOHOL ISOPROPYL 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.
Package Label Principal Display Panel Carton Label Package Label

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.
Do Not Use Do not use • with electrocautery procedures •In the eyes. If contact occurs, flush eyes with water

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 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 Stop Use if irritation or redness develop.If condition persists consult your health care practicioner.

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 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