73242-1112 NDC - CLOVEDEN TOOTH (SODIUM MONOFLUOROPHOSPHATE)

Drug Information

Product NDC: 73242-1112
Proprietary Name: Cloveden Tooth
Non Proprietary Name: Sodium Monofluorophosphate
Active Ingredient(s): .76 g/100g SODIUM MONOFLUOROPHOSPHATE
Administration Route(s): ORAL
Dosage Form(s): PASTE, DENTIFRICE

Labeler Information

Field Name	Field Value
Labeler Name:	DONG IL PHARMS CO.,LTD
Product Type:	HUMAN OTC DRUG
FDA Application Number:	M021
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	7/1/2024

Package Information

No.	Package Code	Package Description	Billing Unit
1	73242-1112-2	1 TUBE in 1 CARTON (73242-1112-2) / 100 g in 1 TUBE (73242-1112-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	73242-1112	The translation of the dosage form Code submitted by the firm.
PRODUCT TYPE NAME	HUMAN OTC DRUG	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAME	Cloveden Tooth	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	Sodium Monofluorophosphate	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	PASTE, DENTIFRICE	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	7/1/2024
MARKETING CATEGORY NAME	OTC MONOGRAPH DRUG	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBER	M021	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
LABELER NAME	DONG IL PHARMS CO.,LTD	This is the date that the labeler indicates was the start of its marketing of the drug product.
SUBSTANCE NAME	SODIUM MONOFLUOROPHOSPHATE	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
ACTIVE NUMERATOR STRENGTH	.76
ACTIVE INGRED UNIT	g/100g

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This page was last updated on: 11/21/2025

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