Product NDC: | 11822-5020 |
Proprietary Name: | Rite Aid |
Non Proprietary Name: | Fluoride |
Active Ingredient(s): | 5; .24 g/100g; g/100g & nbsp; Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-5020 |
Labeler Name: | Rite Aid |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130603 |
Package NDC: | 11822-5020-9 |
Package Description: | 1 TUBE in 1 CARTON (11822-5020-9) > 113 g in 1 TUBE (11822-5020-2) |
NDC Code | 11822-5020-9 |
Proprietary Name | Rite Aid |
Package Description | 1 TUBE in 1 CARTON (11822-5020-9) > 113 g in 1 TUBE (11822-5020-2) |
Product NDC | 11822-5020 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20130603 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Rite Aid |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 5; .24 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |