Home
>
National Drug Code (NDC)
>
NU-DERM SUN SHIELD SPF 50 SUNSCREEN
NU-DERM SUN SHIELD SPF 50 SUNSCREEN - 62032-124-10 - (ZINC OXIDE and OCTINOXATE)
Drug Information of NU-DERM SUN SHIELD SPF 50 SUNSCREEN
| Product NDC: | 62032-124 |
| Proprietary Name: | NU-DERM SUN SHIELD SPF 50 SUNSCREEN |
| Non Proprietary Name: | ZINC OXIDE and OCTINOXATE |
| Active Ingredient(s): | 75; 105 mg/mL; mg/mL & nbsp; ZINC OXIDE and OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NU-DERM SUN SHIELD SPF 50 SUNSCREEN
| Product NDC: | 62032-124 |
| Labeler Name: | OMP, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110105 |
Package Information of NU-DERM SUN SHIELD SPF 50 SUNSCREEN
| Package NDC: | 62032-124-10 |
| Package Description: | 1 TUBE in 1 CARTON (62032-124-10) > 89 mL in 1 TUBE |
NDC Information of NU-DERM SUN SHIELD SPF 50 SUNSCREEN
| NDC Code | 62032-124-10 |
| Proprietary Name | NU-DERM SUN SHIELD SPF 50 SUNSCREEN |
| Package Description | 1 TUBE in 1 CARTON (62032-124-10) > 89 mL in 1 TUBE |
| Product NDC | 62032-124 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE and OCTINOXATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110105 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OMP, Inc. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 105 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
