| 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 |