| Product NDC: | 42673-001 |
| Proprietary Name: | Epionce Ultra Shield |
| Non Proprietary Name: | Zinc Oxide, Homosalate, Octisalate |
| Active Ingredient(s): | .1; .05; .101 mL/mL; mL/mL; mL/mL & nbsp; Zinc Oxide, Homosalate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42673-001 |
| Labeler Name: | Episciences, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090406 |
| Package NDC: | 42673-001-03 |
| Package Description: | 6 mL in 1 TUBE (42673-001-03) |
| NDC Code | 42673-001-03 |
| Proprietary Name | Epionce Ultra Shield |
| Package Description | 6 mL in 1 TUBE (42673-001-03) |
| Product NDC | 42673-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide, Homosalate, Octisalate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090406 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Episciences, Inc. |
| Substance Name | HOMOSALATE; OCTISALATE; ZINC OXIDE |
| Strength Number | .1; .05; .101 |
| Strength Unit | mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |