Product NDC: | 22912-000 |
Proprietary Name: | fluorodine OXYGEN white Fluoride Anticavity |
Non Proprietary Name: | SODIUM FLUORIDE |
Active Ingredient(s): | .24 g/100g & nbsp; SODIUM FLUORIDE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 22912-000 |
Labeler Name: | Multibrands International Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130327 |
Package NDC: | 22912-000-00 |
Package Description: | 1 TUBE in 1 PACKAGE (22912-000-00) > 132 g in 1 TUBE |
NDC Code | 22912-000-00 |
Proprietary Name | fluorodine OXYGEN white Fluoride Anticavity |
Package Description | 1 TUBE in 1 PACKAGE (22912-000-00) > 132 g in 1 TUBE |
Product NDC | 22912-000 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM FLUORIDE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20130327 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Multibrands International Ltd |
Substance Name | SODIUM FLUORIDE |
Strength Number | .24 |
Strength Unit | g/100g |
Pharmaceutical Classes |