59854-301 NDC - DELUXE ALL-PURPOSE ()

Drug Information

Product NDC: 59854-301

Proprietary Name: DELUXE ALL-PURPOSE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Johnson Labs, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2000

Package Information

No. Package Code Package Description Billing Unit
159854-301-013.78 L in 1 BOTTLE (59854-301-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59854-301The 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 NAMEDELUXE ALL-PURPOSEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2000This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEJohnson Labs, Inc.Name 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