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Alcohol pad - Medication Information

Product NDC Code 72459-014
Drug Name

Alcohol pad

Type Brand
Active Ingredients
Isopropyl alcohol 70 ml/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 797544
Application Number 505G(a)(3)
Labeler Name Yiwu Ori-Power Medtech Co.,Ltd.
Packages
Package NDC Code Description
72459-014-01 1 pouch in 1 box (72459-014-01) / .34 ml in 1 pouch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Isopropyl Alcohol 70%v/v. Purpose First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

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 Tear open packet, use alcohol pad to cleanse desired skin area or surfaces. Discard pad appropriately after use.

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.
Use Cleaning and preparing skin for medical procedures.

Purpose

Information about the drug product’s indications for use.
Purpose First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

Spl product data elements

Usually a list of ingredients in a drug product.
Alcohol Pad ISOPROPYL ALCOHOL 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 Labeling: 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.
DRUG FACTS Storage Store at room temperature 15°C-30°C (59°F-56°F).

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 with electocautery procedures.

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 In case of accidental swallowing, seek medical help and contact poison control immediately.

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. Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If irritation develops for more than 72 hours, consult physician. Do not use with electocautery procedures. Keep Out Of Reach Of Children In case of accidental swallowing, seek medical help and contact poison control immediately.

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