Product NDC: | 47649-5001 |
Proprietary Name: | BlancTis Forte II |
Non Proprietary Name: | alcohol |
Active Ingredient(s): | 500 mg/g & nbsp; alcohol |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47649-5001 |
Labeler Name: | Nibec Co., Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100724 |
Package NDC: | 47649-5001-4 |
Package Description: | 2 CARTON in 1 CARTON (47649-5001-4) > 4 TUBE in 1 CARTON (47649-5001-3) > 3 g in 1 TUBE (47649-5001-2) |
NDC Code | 47649-5001-4 |
Proprietary Name | BlancTis Forte II |
Package Description | 2 CARTON in 1 CARTON (47649-5001-4) > 4 TUBE in 1 CARTON (47649-5001-3) > 3 g in 1 TUBE (47649-5001-2) |
Product NDC | 47649-5001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | alcohol |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20100724 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Nibec Co., Ltd |
Substance Name | ALCOHOL |
Strength Number | 500 |
Strength Unit | mg/g |
Pharmaceutical Classes |