| Product NDC: | 0041-0350 |
| Proprietary Name: | Oral-B Fluorinse Mint |
| Non Proprietary Name: | Oral-B Fluorinse Mint |
| Active Ingredient(s): | 2 mg/mL & nbsp; Oral-B Fluorinse Mint |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0041-0350 |
| Labeler Name: | Oral-B Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000504 |
| Package NDC: | 0041-0350-07 |
| Package Description: | 500 mL in 1 BOTTLE, PLASTIC (0041-0350-07) |
| NDC Code | 0041-0350-07 |
| Proprietary Name | Oral-B Fluorinse Mint |
| Package Description | 500 mL in 1 BOTTLE, PLASTIC (0041-0350-07) |
| Product NDC | 0041-0350 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oral-B Fluorinse Mint |
| Dosage Form Name | MOUTHWASH |
| Route Name | DENTAL |
| Start Marketing Date | 20000504 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Oral-B Laboratories |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |