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 |