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