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BlancTis Forte II
BlancTis Forte II - 47649-5001-1 - (alcohol)
Drug Information of BlancTis Forte II
| 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) |
Labeler Information of BlancTis Forte II
| 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 Information of BlancTis Forte II
| Package NDC: | 47649-5001-1 |
| Package Description: | 5 g in 1 TUBE (47649-5001-1) |
NDC Information of BlancTis Forte II
| NDC Code | 47649-5001-1 |
| Proprietary Name | BlancTis Forte II |
| Package Description | 5 g in 1 TUBE (47649-5001-1) |
| 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 |
