NDC 70000-0020 Ethyl Rubbing Alcohol

Isopropyl Alcohol

NDC Product Code 70000-0020

NDC 70000-0020-1

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Ethyl Rubbing Alcohol with NDC 70000-0020 is a a human over the counter drug product labeled by Cardinal Health. The generic name of Ethyl Rubbing Alcohol is isopropyl alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Cardinal Health

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Ethyl Rubbing Alcohol Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ISOPROPYL ALCOHOL 610 mg/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ACETONE (UNII: 1364PS73AF)
  • DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
  • METHYL ISOBUTYL KETONE (UNII: U5T7B88CNP)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Cardinal Health
Labeler Code: 70000
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-18-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Ethyl Rubbing Alcohol Product Label Images

Ethyl Rubbing Alcohol Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Ethyl alcohol 70%

Purpose

First aid antiseptic

Use

Helps prevent the risk of infection in:•minor cuts • scrapes •burns

Warnings

For external use only

Flammable

Keep away from fire or flame, heat, spark, electrical

Ask A Doctor Before Use If You Have

Deep or puncture wounds, animal bites or serious burns

When Using This Product

  • Do not get into eyesdo not apply over large areas of the bodydo not use longer than 1 week

Stop Use And Ask A Doctor If

Condition persists or gets worse

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

For Rubbing & Massaging:

Caution - Fumes can be acutely irritating to skin, eyes and the respiratoruy system.  Do not apply to irritated skine or if excessive irritation developt.  Avoid getting into the eyes or on mucous membranes.  Avoid inhaling this product

Directions

  • Clean the affected areaapply a small amount of this product on the affected area 1 to 3 times dailymay be covered with a sterile bandageif bandaged, let dry first

Other Information

  • Will produce serious gastric disturbances if taken internally

Inactive Ingredients

Acetone, denatonium benzoate, methyl isobutyl ketone, water

Adverse Reactions Section

DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017CIN 2369411  www.myleader.com  1-800-200-6313876.002/876AC

* Please review the disclaimer below.

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