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BlancTis Essence
BlancTis Essence - 47649-4001-2 - (alcohol)
Drug Information of BlancTis Essence
| Product NDC: | 47649-4001 |
| Proprietary Name: | BlancTis Essence |
| 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 Essence
| Product NDC: | 47649-4001 |
| Labeler Name: | Nibec Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100305 |
Package Information of BlancTis Essence
| Package NDC: | 47649-4001-2 |
| Package Description: | 12 TUBE in 1 CARTON (47649-4001-2) > 3.5 g in 1 TUBE (47649-4001-1) |
NDC Information of BlancTis Essence
| NDC Code | 47649-4001-2 |
| Proprietary Name | BlancTis Essence |
| Package Description | 12 TUBE in 1 CARTON (47649-4001-2) > 3.5 g in 1 TUBE (47649-4001-1) |
| Product NDC | 47649-4001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | alcohol |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20100305 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Nibec Co., Ltd |
| Substance Name | ALCOHOL |
| Strength Number | 500 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
