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Alcohol prep pads - Medication Information

Product NDC Code 77133-000
Drug Name

Alcohol prep pads

Type Brand
Active Ingredients
Isopropyl alcohol .7 ml/ml
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 797544
Application Number 505G(a)(3)
Labeler Name ALCOVE BRANDS
Packages
Package NDC Code Description
77133-000-00 100 patch in 1 box (77133-000-00) / .4 ml in 1 patch
77133-000-01 200 patch in 1 box (77133-000-01) / .4 ml in 1 patch
77133-000-02 300 patch in 1 box (77133-000-02) / .4 ml in 1 patch
77133-000-03 400 patch in 1 box (77133-000-03) / .4 ml in 1 patch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Isopropyl Alcohol 70% v/v Purpose Antiseptic

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. Discard after single use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredient 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 for the preparation of skin prior to injection and to decrease germs in minor cuts and scrapes. Non-sterile Solution Applicator is sterile if package is intact.

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.
Alcohol Prep Pads 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:77133-000-00 Bottle Package Labeling:77133-000-01 Bottle2 Package Labeling:77133-000-02 Bottle3 Package Labeling:77133-000-03 Bottle4

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

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 except with adult supervision. If swallowed, get medical help or contact a Poison Control Cenre 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 develops.

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 flame or fire. Stop use and ask a doctor if irritation develops. Keep out of reach of children except with adult supervision. If swallowed, get medical help or contact a Poison Control Cenre 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