NDC 73921-038 L-topical 50% Isopropyl Rubbing Alcohol

Isopropyl Alcohol

NDC Product Code 73921-038

NDC CODE: 73921-038

Proprietary Name: L-topical 50% Isopropyl Rubbing 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

  • 73921 - Global Pharma Healthcare Private Limited
    • 73921-038 - L-topical 50% Isopropyl Rubbing Alcohol

NDC 73921-038-16

Package Description: 474 mL in 1 CONTAINER

NDC Product Information

L-topical 50% Isopropyl Rubbing Alcohol with NDC 73921-038 is a a human over the counter drug product labeled by Global Pharma Healthcare Private Limited. The generic name of L-topical 50% Isopropyl Rubbing Alcohol is isopropyl alcohol. The product's dosage form is solution and is administered via topical form.

Labeler Name: Global Pharma Healthcare Private Limited

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.

L-topical 50% Isopropyl 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.


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: Global Pharma Healthcare Private Limited
Labeler Code: 73921
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: 04-01-2021 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: 12-31-2022 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".

* Please review the disclaimer below.

L-topical 50% Isopropyl Rubbing Alcohol Product Label Images

L-topical 50% Isopropyl 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

Isopropyl alcohol (50%)


First Aid Antiseptic


First aid to help prevent the risk of infection in minor cuts, scrapes and burns


For external use only• Flammable, keep away from fire and flame• If taken internally, serious gastric disturbances will resultAsk a doctor before use in you have • deep or puncture wounds, animal bites or serious burnsWhen using this product • do not get into eye • do not apply over large areas of the body • do not use longer than one week unless directed by a doctor • do not use otherwise than directedStop use and ask a doctor if• Condition persists or gets worse

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center immediately.


• clean affected area • apply a small amount of this product on the area 1 to 3 times daily • if bandaged, let dry first • may be covered with a sterile bandage

Other Information

• store at room temperature • does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredient

Purified water

* Please review the disclaimer below.