70201-001 NDC - ISOPROPYL RUBBING ALCOHOL 50% ()

Drug Information

Product NDC: 70201-001

Proprietary Name: Isopropyl Rubbing Alcohol 50%

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: North & South Wholesalers LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/3/2015

Package Information

No. Package Code Package Description Billing Unit
170201-001-01118 mL in 1 BOTTLE, PLASTIC (70201-001-01)
270201-001-02177 mL in 1 BOTTLE, PLASTIC (70201-001-02)
370201-001-03237 mL in 1 BOTTLE, PLASTIC (70201-001-03)
470201-001-04296 mL in 1 BOTTLE, PLASTIC (70201-001-04)
570201-001-05355 mL in 1 BOTTLE, PLASTIC (70201-001-05)
670201-001-06414 mL in 1 BOTTLE, PLASTIC (70201-001-06)
770201-001-07473 mL in 1 BOTTLE, PLASTIC (70201-001-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70201-001The 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 Rubbing Alcohol 50%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 DATE11/3/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENorth & South Wholesalers 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