Product NDC: | 36800-001 |
Proprietary Name: | Mouth Rinse |
Non Proprietary Name: | sodium fluoride |
Active Ingredient(s): | .1 mg/mL & nbsp; sodium fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | MOUTHWASH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 36800-001 |
Labeler Name: | Topco associates LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101230 |
Package NDC: | 36800-001-86 |
Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (36800-001-86) |
NDC Code | 36800-001-86 |
Proprietary Name | Mouth Rinse |
Package Description | 1000 mL in 1 BOTTLE, PLASTIC (36800-001-86) |
Product NDC | 36800-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | sodium fluoride |
Dosage Form Name | MOUTHWASH |
Route Name | ORAL |
Start Marketing Date | 20101230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Topco associates LLC |
Substance Name | SODIUM FLUORIDE |
Strength Number | .1 |
Strength Unit | mg/mL |
Pharmaceutical Classes |