Dentree - 76170-103-01 - (sodium fluoride)

Alphabetical Index


Drug Information of Dentree

Product NDC: 76170-103
Proprietary Name: Dentree
Non Proprietary Name: sodium fluoride
Active Ingredient(s): .22    g/100mL & nbsp;   sodium fluoride
Administration Route(s): DENTAL
Dosage Form(s): GEL, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Dentree

Product NDC: 76170-103
Labeler Name: e-soup Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121201

Package Information of Dentree

Package NDC: 76170-103-01
Package Description: 1 BOTTLE, PUMP in 1 CARTON (76170-103-01) > 30 mL in 1 BOTTLE, PUMP

NDC Information of Dentree

NDC Code 76170-103-01
Proprietary Name Dentree
Package Description 1 BOTTLE, PUMP in 1 CARTON (76170-103-01) > 30 mL in 1 BOTTLE, PUMP
Product NDC 76170-103
Product Type Name HUMAN OTC DRUG
Non Proprietary Name sodium fluoride
Dosage Form Name GEL, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20121201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name e-soup Co., Ltd.
Substance Name SODIUM FLUORIDE
Strength Number .22
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Dentree


General Information