37000-993 NDC - CREST PREMIUM PLUS ()

Drug Information

Product NDC: 37000-993

Proprietary Name: Crest Premium Plus

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: The Procter & Gamble Manufacturing Company
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2021

Package Information

No. Package Code Package Description Billing Unit
137000-993-521 TUBE in 1 CARTON (37000-993-52) / 147 g in 1 TUBE
237000-993-721 TUBE in 1 CARTON (37000-993-72) / 204 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC37000-993The 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 NAMECrest Premium PlusThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXAdvanced Whitening Active FoamA 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 DATE1/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEThe Procter & Gamble Manufacturing CompanyName 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