11084-115 NDC - PANACHE ()

Drug Information

Product NDC: 11084-115

Proprietary Name: Panache

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Deb USA, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2010

Package Information

No. Package Code Package Description Billing Unit
111084-115-053780 mL in 1 BOTTLE, PLASTIC (11084-115-05)
211084-115-072000 mL in 1 CARTRIDGE (11084-115-07)
311084-115-271000 mL in 1 CARTRIDGE (11084-115-27)
411084-115-34118 mL in 1 BOTTLE, PLASTIC (11084-115-34)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11084-115The 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 NAMEPanacheThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXAntibacterial Body WashA 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 DATE1/1/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDeb USA, 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