Product NDC: | 51143-966 |
Proprietary Name: | Anticavity |
Non Proprietary Name: | Sdoium Fluoride |
Active Ingredient(s): | .0221 mL/100L & nbsp; Sdoium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | MOUTHWASH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51143-966 |
Labeler Name: | Onpoint, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120321 |
Package NDC: | 51143-966-86 |
Package Description: | 1 L in 1 BOTTLE, PLASTIC (51143-966-86) |
NDC Code | 51143-966-86 |
Proprietary Name | Anticavity |
Package Description | 1 L in 1 BOTTLE, PLASTIC (51143-966-86) |
Product NDC | 51143-966 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sdoium Fluoride |
Dosage Form Name | MOUTHWASH |
Route Name | ORAL |
Start Marketing Date | 20120321 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Onpoint, Inc |
Substance Name | SODIUM FLUORIDE |
Strength Number | .0221 |
Strength Unit | mL/100L |
Pharmaceutical Classes |