| Product NDC: | 0126-0135 |
| Proprietary Name: | Phos-Flur Ortho Defense |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 4.42 mg/10mL & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0126-0135 |
| Labeler Name: | Colgate Oral Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110112 |
| Package NDC: | 0126-0135-16 |
| Package Description: | 473 mL in 1 BOTTLE (0126-0135-16) |
| NDC Code | 0126-0135-16 |
| Proprietary Name | Phos-Flur Ortho Defense |
| Package Description | 473 mL in 1 BOTTLE (0126-0135-16) |
| Product NDC | 0126-0135 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | RINSE |
| Route Name | DENTAL |
| Start Marketing Date | 20110112 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Colgate Oral Pharmaceuticals, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 4.42 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |