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O BlancTis
O BlancTis - 47649-6001-2 - (alcohol)
Drug Information of O BlancTis
| Product NDC: | 47649-6001 |
| Proprietary Name: | O BlancTis |
| Non Proprietary Name: | alcohol |
| Active Ingredient(s): | 50 g/100g & nbsp; alcohol |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of O BlancTis
| Product NDC: | 47649-6001 |
| Labeler Name: | Nibec Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120207 |
Package Information of O BlancTis
| Package NDC: | 47649-6001-2 |
| Package Description: | 3 TUBE in 1 BOX (47649-6001-2) > 5 g in 1 TUBE (47649-6001-1) |
NDC Information of O BlancTis
| NDC Code | 47649-6001-2 |
| Proprietary Name | O BlancTis |
| Package Description | 3 TUBE in 1 BOX (47649-6001-2) > 5 g in 1 TUBE (47649-6001-1) |
| Product NDC | 47649-6001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | alcohol |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20120207 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Nibec Co., Ltd |
| Substance Name | ALCOHOL |
| Strength Number | 50 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
