Product NDC: | 37000-697 |
Proprietary Name: | Crest Pro-Health |
Non Proprietary Name: | Stannous Fluoride |
Active Ingredient(s): | .00454 mg/g & nbsp; Stannous Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-697 |
Labeler Name: | The Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100315 |
Package NDC: | 37000-697-01 |
Package Description: | 1 TUBE in 1 CARTON (37000-697-01) > .85 g in 1 TUBE |
NDC Code | 37000-697-01 |
Proprietary Name | Crest Pro-Health |
Package Description | 1 TUBE in 1 CARTON (37000-697-01) > .85 g in 1 TUBE |
Product NDC | 37000-697 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Stannous Fluoride |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20100315 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | The Procter & Gamble Manufacturing Company |
Substance Name | STANNOUS FLUORIDE |
Strength Number | .00454 |
Strength Unit | mg/g |
Pharmaceutical Classes |