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UP and UP
UP and UP - 11673-332-04 - (ZINC OXIDE)
Drug Information of UP and UP
| Product NDC: | 11673-332 |
| Proprietary Name: | UP and UP |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 13 g/100g & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UP and UP
| Product NDC: | 11673-332 |
| Labeler Name: | TARGET CORPORATION |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120423 |
Package Information of UP and UP
| Package NDC: | 11673-332-04 |
| Package Description: | 113.3 g in 1 TUBE (11673-332-04) |
NDC Information of UP and UP
| NDC Code | 11673-332-04 |
| Proprietary Name | UP and UP |
| Package Description | 113.3 g in 1 TUBE (11673-332-04) |
| Product NDC | 11673-332 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120423 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TARGET CORPORATION |
| Substance Name | ZINC OXIDE |
| Strength Number | 13 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
