0041-1420 NDC - ORAL-B ()

Drug Information

Product NDC: 0041-1420

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
10041-1420-16500 mL in 1 BOTTLE, PLASTIC (0041-1420-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0041-1420The 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 SUFFIXAnti-BacterialA 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: 9/15/2022