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0041-1421 NDC - ORAL-B ()

Drug Information

Product NDC: 0041-1421

Proprietary Name: Oral-B

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Oral-B Laboratories
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/15/2005

Package Information

No. Package Code Package Description Billing Unit
10041-1421-16500 mL in 1 BOTTLE, PLASTIC (0041-1421-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0041-1421The 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 NAMEOral-BThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXAnticavityA 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 DATE10/15/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOral-B LaboratoriesName 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