Product NDC: | 63868-172 |
Proprietary Name: | Quality Choice |
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: | 63868-172 |
Labeler Name: | CHAIN DRUG MARKETING ASSOCIATION INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110120 |
Package NDC: | 63868-172-29 |
Package Description: | 1 TUBE in 1 CARTON (63868-172-29) > 128 g in 1 TUBE (63868-172-22) |
NDC Code | 63868-172-29 |
Proprietary Name | Quality Choice |
Package Description | 1 TUBE in 1 CARTON (63868-172-29) > 128 g in 1 TUBE (63868-172-22) |
Product NDC | 63868-172 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20110120 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CHAIN DRUG MARKETING ASSOCIATION INC |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 5; .24 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |