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):

No.	Package Code	Package Description	Billing Unit
1	0041-1421-16	500 mL in 1 BOTTLE, PLASTIC (0041-1421-16)

Field Name	Field Value	Definition
PRODUCT NDC	0041-1421	The 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 NAME	Oral-B	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	Anticavity	A 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 DATE	10/15/2005	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Oral-B Laboratories	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