10733-130 NDC - FLUORISHIELD ()

Drug Information

Product NDC: 10733-130

Proprietary Name: FluoriSHIELD

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Medical Products Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	11/29/2009

No.	Package Code	Package Description	Billing Unit
1	10733-130-04	66 BOTTLE in 1 CARTON (10733-130-04) / 114 g in 1 BOTTLE	ML

Field Name	Field Value	Definition
PRODUCT NDC	10733-130	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	FluoriSHIELD	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	11/29/2009	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Medical Products Laboratories, Inc.	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