80668-414 NDC - ISOPROPYL ALCOHOL 99% ()

Drug Information

Product NDC: 80668-414

Proprietary Name: Isopropyl Alcohol 99%

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: UBQ Industries, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/20/2020

Package Information

No. Package Code Package Description Billing Unit
180668-414-0118927 mL in 1 PAIL (80668-414-01)
280668-414-023785 mL in 1 BOTTLE, PLASTIC (80668-414-02)
380668-414-031892 mL in 1 BOTTLE, PLASTIC (80668-414-03)
480668-414-04473.2 mL in 1 BOTTLE, PLASTIC (80668-414-04)
580668-414-05236 mL in 1 BOTTLE (80668-414-05)
680668-414-06946.4 mL in 1 JUG (80668-414-06)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80668-414The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEIsopropyl Alcohol 99%The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/20/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUBQ Industries, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023