37000-875 NDC - CREST 3D WHITE ()

Drug Information

Product NDC: 37000-875

Proprietary Name: Crest 3D White

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:1/18/2016

Package Information

No. Package Code Package Description Billing Unit
137000-875-022 TUBE in 1 CARTON (37000-875-02) / 107 g in 1 TUBE
237000-875-271 TUBE in 1 CARTON (37000-875-27) / 76 g in 1 TUBE
337000-875-301 TUBE in 1 CARTON (37000-875-30) / 85 g in 1 TUBE
437000-875-333 CARTON in 1 CELLO PACK (37000-875-33) / 1 TUBE in 1 CARTON / 107 g in 1 TUBE
537000-875-381 TUBE in 1 CARTON (37000-875-38) / 107 g in 1 TUBE
637000-875-411 TUBE in 1 CARTON (37000-875-41) / 116 g in 1 TUBE
737000-875-501 TUBE in 1 CARTON (37000-875-50) / 141 g in 1 TUBE
837000-875-541 TUBE in 1 CARTON (37000-875-54) / 153 g in 1 TUBE
937000-875-822 CARTON in 1 CELLO PACK (37000-875-82) / 1 TUBE in 1 CARTON / 116 g in 1 TUBE
1037000-875-993 CARTON in 1 CELLO PACK (37000-875-99) / 1 TUBE in 1 CARTON / 116 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC37000-875The 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 WhiteThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXArctic FreshA 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 DATE1/18/2016This 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