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NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50
NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50 - 62032-104-90 - (OCTINOXATE and ZINC OXIDE)
Drug Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50
| Product NDC: | 62032-104 |
| Proprietary Name: | NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50 |
| Non Proprietary Name: | OCTINOXATE and ZINC OXIDE |
| Active Ingredient(s): | 75; 105 mg/g; mg/g & nbsp; OCTINOXATE and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50
| Product NDC: | 62032-104 |
| Labeler Name: | OMP, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121107 |
Package Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50
| Package NDC: | 62032-104-90 |
| Package Description: | 85 g in 1 TUBE (62032-104-90) |
NDC Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50
| NDC Code | 62032-104-90 |
| Proprietary Name | NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50 |
| Package Description | 85 g in 1 TUBE (62032-104-90) |
| Product NDC | 62032-104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121107 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OMP, Inc. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 105 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
