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Epionce Ultra Shield - 42673-001-04 - (Zinc Oxide, Homosalate, Octisalate)

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Drug Information of Epionce Ultra Shield

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)

Labeler Information of Epionce Ultra Shield

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 Information of Epionce Ultra Shield

Package NDC: 42673-001-04
Package Description: 453 mL in 1 JAR (42673-001-04)

NDC Information of Epionce Ultra Shield

NDC Code 42673-001-04
Proprietary Name Epionce Ultra Shield
Package Description 453 mL in 1 JAR (42673-001-04)
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

Complete Information of Epionce Ultra Shield


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