72934-2059 NDC - CLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4% ()

Drug Information

Product NDC: 72934-2059

Proprietary Name: CLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4%

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sincerus Florida, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2019

Package Information

No. Package Code Package Description Billing Unit
172934-2059-360 g in 1 BOTTLE, PUMP (72934-2059-3)GM

NDC Record

Field Name Field Value Definition
PRODUCT NDC72934-2059The 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 NAMECLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4%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 DATE5/1/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESincerus Florida, 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