Product NDC: | 51442-546 |
Proprietary Name: | COLGATE |
Non Proprietary Name: | SODIUM FLUORIDE |
Active Ingredient(s): | 2.4 mg/g & nbsp; SODIUM FLUORIDE |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51442-546 |
Labeler Name: | Colgate-Palmolive Canada |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101110 |
Package NDC: | 51442-546-66 |
Package Description: | 1 TUBE in 1 CARTON (51442-546-66) > 164 g in 1 TUBE |
NDC Code | 51442-546-66 |
Proprietary Name | COLGATE |
Package Description | 1 TUBE in 1 CARTON (51442-546-66) > 164 g in 1 TUBE |
Product NDC | 51442-546 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM FLUORIDE |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20101110 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Colgate-Palmolive Canada |
Substance Name | SODIUM FLUORIDE |
Strength Number | 2.4 |
Strength Unit | mg/g |
Pharmaceutical Classes |