| Product NDC: | 36800-001 |
| Proprietary Name: | Mouth Rinse |
| Non Proprietary Name: | sodium fluoride |
| Active Ingredient(s): | .1 mg/mL & nbsp; sodium fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 36800-001 |
| Labeler Name: | Topco associates LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101230 |
| Package NDC: | 36800-001-86 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (36800-001-86) |
| NDC Code | 36800-001-86 |
| Proprietary Name | Mouth Rinse |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (36800-001-86) |
| Product NDC | 36800-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium fluoride |
| Dosage Form Name | MOUTHWASH |
| Route Name | ORAL |
| Start Marketing Date | 20101230 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Topco associates LLC |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |