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: | 64893-300-01 |
Package Description: | 473 mL in 1 TUBE (64893-300-01) |
NDC Code | 64893-300-01 |
Proprietary Name | Firefly Mouth Swoosh Anti-Cavity Fluoride Rinse |
Package Description | 473 mL in 1 TUBE (64893-300-01) |
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 |