Product NDC: | 62032-200 |
Proprietary Name: | NU-DERM HEALTHY SKIN PROTECTION |
Non Proprietary Name: | OCTINOXATE and ZINC OXIDE |
Active Ingredient(s): | 75; 90 mg/mL; mg/mL & nbsp; OCTINOXATE and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62032-200 |
Labeler Name: | OMP, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20020101 |
Package NDC: | 62032-200-10 |
Package Description: | 30 mL in 1 BOTTLE, PLASTIC (62032-200-10) |
NDC Code | 62032-200-10 |
Proprietary Name | NU-DERM HEALTHY SKIN PROTECTION |
Package Description | 30 mL in 1 BOTTLE, PLASTIC (62032-200-10) |
Product NDC | 62032-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and ZINC OXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20020101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | OMP, Inc. |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 75; 90 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |