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SUPER BB
SUPER BB - 50556-001-01 - (TITANIUM DIOXIDE)
Drug Information of SUPER BB
| Product NDC: | 50556-001 |
| Proprietary Name: | SUPER BB |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 1.6 mL/30mL & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUPER BB
| Product NDC: | 50556-001 |
| Labeler Name: | UNHWA CORPORATION |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090401 |
Package Information of SUPER BB
| Package NDC: | 50556-001-01 |
| Package Description: | 30 mL in 1 CARTON (50556-001-01) |
NDC Information of SUPER BB
| NDC Code | 50556-001-01 |
| Proprietary Name | SUPER BB |
| Package Description | 30 mL in 1 CARTON (50556-001-01) |
| Product NDC | 50556-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20090401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | UNHWA CORPORATION |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 1.6 |
| Strength Unit | mL/30mL |
| Pharmaceutical Classes |
