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U-max Multi BB
U-max Multi BB - 50795-2001-1 - (ALLANTOIN)
Drug Information of U-max Multi BB
| Product NDC: | 50795-2001 |
| Proprietary Name: | U-max Multi BB |
| Non Proprietary Name: | ALLANTOIN |
| Active Ingredient(s): | .1 mL/100mL & nbsp; ALLANTOIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of U-max Multi BB
| Product NDC: | 50795-2001 |
| Labeler Name: | VS Shinbi Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120604 |
Package Information of U-max Multi BB
| Package NDC: | 50795-2001-1 |
| Package Description: | 30 mL in 1 BOTTLE, WITH APPLICATOR (50795-2001-1) |
NDC Information of U-max Multi BB
| NDC Code | 50795-2001-1 |
| Proprietary Name | U-max Multi BB |
| Package Description | 30 mL in 1 BOTTLE, WITH APPLICATOR (50795-2001-1) |
| Product NDC | 50795-2001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALLANTOIN |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120604 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | VS Shinbi Co., Ltd. |
| Substance Name | ALLANTOIN |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
