NDC 73598-0651 Isopropyl Alcohol
Isopropyl Alcohol
NDC Product Code 73598-0651
Proprietary Name: Isopropyl Alcohol What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Isopropyl Alcohol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 73598 - Jhk Inc
- 73598-0651 - Isopropyl Alcohol
NDC 73598-0651-1
Package Description: .0591 L in 1 BOTTLE, SPRAY
NDC Product Information
Isopropyl Alcohol with NDC 73598-0651 is a a human over the counter drug product labeled by Jhk Inc. The generic name of Isopropyl Alcohol is isopropyl alcohol. The product's dosage form is spray and is administered via topical form.
Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.
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.
Isopropyl 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.
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.
- 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: Jhk Inc
Labeler Code: 73598
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: 02-14-2020 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: 12-31-2021 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
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Isopropyl Alcohol Product Label Images
Isopropyl 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
- Other
- Active Ingredient
- Purpose
- Uses
- Warnings
- Do Not Use
- Otc - Keep Out Of Reach Of Children
- Otc - Stop Use
- Directions
- Other Information
- Inactive Ingredients
- Questions?
Other
Drug Facts
Active Ingredient
Isopropyl Alcohol 70%
Purpose
First aid antiseptic
Uses
First aid to help prevent infection in minor cuts, scrapes and burns.
Warnings
For external use only. Flammable keep away from fire or flame.
Do Not Use
- Near eyes or mucous membranes
- On deep or puncture wounds, animal bites or serious burns
- Over large areas of the body
- More than one week unless directed by a doctor
Otc - 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.
Otc - Stop Use
Stop use and ask a doctor if conditions persist or get worse.
Directions
- Clean the affected area
- Apply a small amount of this product on the area 1 - 3 times daily
- Children under 2 ask a doctor
Other Information
- Store at room temperature
Inactive Ingredients
Purified water
Questions?
1-866-651-3660
Mon-Fri 8:00am-5:00pm EST
Manufactured for American Safety & First Aid Osceola, IN 46561
* Please review the disclaimer below.