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Conju Princess BB
Conju Princess BB - 59915-1001-1 - (arbutin)
Drug Information of Conju Princess BB
| Product NDC: | 59915-1001 |
| Proprietary Name: | Conju Princess BB |
| Non Proprietary Name: | arbutin |
| Active Ingredient(s): | .04; 2; 10.15 mL/100mL; mL/100mL; mL/100mL & nbsp; arbutin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Conju Princess BB
| Product NDC: | 59915-1001 |
| Labeler Name: | Conju Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110124 |
Package Information of Conju Princess BB
| Package NDC: | 59915-1001-1 |
| Package Description: | 30 mL in 1 TUBE (59915-1001-1) |
NDC Information of Conju Princess BB
| NDC Code | 59915-1001-1 |
| Proprietary Name | Conju Princess BB |
| Package Description | 30 mL in 1 TUBE (59915-1001-1) |
| Product NDC | 59915-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | arbutin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110124 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Conju Inc |
| Substance Name | ADENOSINE; ARBUTIN; TITANIUM DIOXIDE |
| Strength Number | .04; 2; 10.15 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
