37000-215 NDC - CREST 3D WHITE WHITENING THERAPY ()

Drug Information

Product NDC: 37000-215

Proprietary Name: Crest 3D White Whitening Therapy

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Procter & Gamble Manfuacturing Company
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2019

Package Information

No. Package Code Package Description Billing Unit
137000-215-033 CARTON in 1 CELLO PACK (37000-215-03) / 1 TUBE in 1 CARTON / 147 g in 1 TUBE
237000-215-044 CARTON in 1 CELLO PACK (37000-215-04) / 1 TUBE in 1 CARTON / 147 g in 1 TUBE
337000-215-281 TUBE in 1 CARTON (37000-215-28) / 79 g in 1 TUBE
437000-215-411 TUBE in 1 CARTON (37000-215-41) / 116 g in 1 TUBE
537000-215-521 TUBE in 1 CARTON (37000-215-52) / 147 g in 1 TUBE
637000-215-822 CARTON in 1 CELLO PACK (37000-215-82) / 1 TUBE in 1 CARTON / 116 g in 1 TUBE
737000-215-851 TUBE in 1 CARTON (37000-215-85) / 24 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC37000-215The 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 3D White Whitening TherapyThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXDeep Clean CharcoalA 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 DATE1/1/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEProcter & Gamble Manfuacturing 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