Product NDC: | 51143-213 |
Proprietary Name: | Anticavity Fluoride Rinse |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | .05 kg/100L & nbsp; Sodium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | MOUTHWASH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51143-213 |
Labeler Name: | The Great Atlantic + Pacific Tea Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101112 |
Package NDC: | 51143-213-44 |
Package Description: | .532 L in 1 BOTTLE, PLASTIC (51143-213-44) |
NDC Code | 51143-213-44 |
Proprietary Name | Anticavity Fluoride Rinse |
Package Description | .532 L in 1 BOTTLE, PLASTIC (51143-213-44) |
Product NDC | 51143-213 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | MOUTHWASH |
Route Name | ORAL |
Start Marketing Date | 20101112 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | The Great Atlantic + Pacific Tea Company |
Substance Name | SODIUM FLUORIDE |
Strength Number | .05 |
Strength Unit | kg/100L |
Pharmaceutical Classes |