| Product NDC: | 61481-0037 |
| Proprietary Name: | KINeSYS EarthKind SPF 30 Sunscreen |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 250 g/1000g & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61481-0037 |
| Labeler Name: | KINeSYS Pharmaceutical Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110201 |
| Package NDC: | 61481-0037-3 |
| Package Description: | 90 g in 1 JAR (61481-0037-3) |
| NDC Code | 61481-0037-3 |
| Proprietary Name | KINeSYS EarthKind SPF 30 Sunscreen |
| Package Description | 90 g in 1 JAR (61481-0037-3) |
| Product NDC | 61481-0037 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KINeSYS Pharmaceutical Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 250 |
| Strength Unit | g/1000g |
| Pharmaceutical Classes |