Home
>
National Drug Code (NDC)
>
COLGATE PROCLINICAL - SPARKLING MINT
COLGATE PROCLINICAL - SPARKLING MINT - 51442-543-69 - (SODIUM FLUORIDE)
Drug Information of COLGATE PROCLINICAL - SPARKLING MINT
| Product NDC: | 51442-543 |
| Proprietary Name: | COLGATE PROCLINICAL - SPARKLING MINT |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 2.4 mg/g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of COLGATE PROCLINICAL - SPARKLING MINT
| Product NDC: | 51442-543 |
| Labeler Name: | Colgate-Palmolive Canada |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101110 |
Package Information of COLGATE PROCLINICAL - SPARKLING MINT
| Package NDC: | 51442-543-69 |
| Package Description: | 1 TUBE in 1 CARTON (51442-543-69) > 113 g in 1 TUBE |
NDC Information of COLGATE PROCLINICAL - SPARKLING MINT
| NDC Code | 51442-543-69 |
| Proprietary Name | COLGATE PROCLINICAL - SPARKLING MINT |
| Package Description | 1 TUBE in 1 CARTON (51442-543-69) > 113 g in 1 TUBE |
| Product NDC | 51442-543 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | PASTE, 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 |
