| Product NDC: | 62032-119 |
| Proprietary Name: | CONDITION AND ENHANCE 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: | 62032-119 |
| Labeler Name: | OMP, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20020101 |
| Package NDC: | 62032-119-10 |
| Package Description: | 30 mL in 1 BOTTLE, PLASTIC (62032-119-10) |
| NDC Code | 62032-119-10 |
| Proprietary Name | CONDITION AND ENHANCE HEALTHY SKIN PROTECTION |
| Package Description | 30 mL in 1 BOTTLE, PLASTIC (62032-119-10) |
| Product NDC | 62032-119 |
| 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 |