| Product NDC: | 64893-300 |
| Proprietary Name: | Firefly Mouth Swoosh Anti-Cavity Fluoride Rinse |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .05 mL/100mL & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64893-300 |
| Labeler Name: | Dr. Fresh, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100902 |
| Package NDC: | 64893-300-00 |
| Package Description: | 44 mL in 1 TUBE (64893-300-00) |
| NDC Code | 64893-300-00 |
| Proprietary Name | Firefly Mouth Swoosh Anti-Cavity Fluoride Rinse |
| Package Description | 44 mL in 1 TUBE (64893-300-00) |
| Product NDC | 64893-300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | LIQUID |
| Route Name | DENTAL |
| Start Marketing Date | 20100902 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dr. Fresh, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .05 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |