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 |