| Product NDC: | 37000-003 |
| Proprietary Name: | Crest Pro-Health |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .0219 g/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37000-003 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100816 |
| Package NDC: | 37000-003-01 |
| Package Description: | 500 mL in 1 BOTTLE, PLASTIC (37000-003-01) |
| NDC Code | 37000-003-01 |
| Proprietary Name | Crest Pro-Health |
| Package Description | 500 mL in 1 BOTTLE, PLASTIC (37000-003-01) |
| Product NDC | 37000-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | RINSE |
| Route Name | ORAL |
| Start Marketing Date | 20100816 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .0219 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |