NDC 50730-3002 Isopropyl Alcohol

NDC Product Code 50730-3002

NDC CODE: 50730-3002

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.

NDC Code Structure

NDC 50730-3002-0

Package Description: 100 PACKET in 1 BOX > 1 SWAB in 1 PACKET

NDC 50730-3002-1

Package Description: 4000 PACKET in 1 CASE > 1 SWAB in 1 PACKET

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Isopropyl Alcohol with NDC 50730-3002 is a product labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 797544.

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)

Product Labeler Information

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

Labeler Name: H And P Industries, Inc. Dba Triad Group
Labeler Code: 50730
Start Marketing Date: 05-01-1986 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

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

Active Ingredient

Isopropyl Alcohol 70% v/v




  • For preparation of the skin prior to injection


  • For external use onlyFlammable, keep away from fire or flame

Do Not Use

  • With electrocautery proceduresIn the eyes

Stop Use

If irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Keep Out Of Reach Of Children

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


Wipe injection site vigorously and discard.

Other Information

Store at room temperature 15°- 30° C (59° - 86° F)

Inactive Ingredient

Purified water

Package Information

TRIADCat. No. 10-3002NDC 50730-3002-0Alcohol Prep Pads, LargeAntiseptic for preparation of the skin prior to injection70% Isopropyl Alcohol, v/v100 Prep PadsTriad Group, Inc.700 West North Shore DriveHartland, WI 53029MADE IN USAwww.triad-group.net1-800-288-1288

* Please review the disclaimer below.