OMNI - 48878-4021-3 - (stannous fluoride)

Alphabetical Index


Drug Information of OMNI

Product NDC: 48878-4021
Proprietary Name: OMNI
Non Proprietary Name: stannous fluoride
Active Ingredient(s): 4    mg/g & nbsp;   stannous fluoride
Administration Route(s): ORAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of OMNI

Product NDC: 48878-4021
Labeler Name: 3M ESPE Dental Products
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19980201

Package Information of OMNI

Package NDC: 48878-4021-3
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (48878-4021-3) > 121.9 g in 1 BOTTLE, PLASTIC

NDC Information of OMNI

NDC Code 48878-4021-3
Proprietary Name OMNI
Package Description 1 BOTTLE, PLASTIC in 1 BOX (48878-4021-3) > 121.9 g in 1 BOTTLE, PLASTIC
Product NDC 48878-4021
Product Type Name HUMAN OTC DRUG
Non Proprietary Name stannous fluoride
Dosage Form Name GEL
Route Name ORAL
Start Marketing Date 19980201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name 3M ESPE Dental Products
Substance Name STANNOUS FLUORIDE
Strength Number 4
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of OMNI


General Information