52920-130 NDC - ISOPROPYL RUBBING ALCOHOL 50% ()

Drug Information

Product NDC: 52920-130

Proprietary Name: ISOPROPYL RUBBING ALCOHOL 50%

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Singhfam Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/10/2015

Package Information

No. Package Code Package Description Billing Unit
152920-130-41118 mL in 1 BOTTLE, PLASTIC (52920-130-41)
252920-130-42177 mL in 1 BOTTLE, PLASTIC (52920-130-42)
352920-130-43237 mL in 1 BOTTLE, PLASTIC (52920-130-43)
452920-130-44296 mL in 1 BOTTLE, PLASTIC (52920-130-44)
552920-130-45354 mL in 1 BOTTLE, PLASTIC (52920-130-45)
652920-130-46414 mL in 1 BOTTLE, PLASTIC (52920-130-46)
752920-130-47473 mL in 1 BOTTLE, PLASTIC (52920-130-47)

NDC Record

Field Name Field Value Definition
PRODUCT NDC52920-130The 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.
PROPRIETARY NAME SUFFIXWITH WINTERGREENA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE8/10/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESinghfam CorporationName 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