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Elta MD UV Aero - 60232-2587-6 - (zinc oxide and octinoxate aerosol)

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Drug Information of Elta MD UV Aero

Product NDC: 60232-2587
Proprietary Name: Elta MD UV Aero
Non Proprietary Name: zinc oxide and octinoxate aerosol
Active Ingredient(s): 75; 93    g/1000g; g/1000g & nbsp;   zinc oxide and octinoxate aerosol
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Elta MD UV Aero

Product NDC: 60232-2587
Labeler Name: Swiss American Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120501

Package Information of Elta MD UV Aero

Package NDC: 60232-2587-6
Package Description: 6 g in 1 CAN (60232-2587-6)

NDC Information of Elta MD UV Aero

NDC Code 60232-2587-6
Proprietary Name Elta MD UV Aero
Package Description 6 g in 1 CAN (60232-2587-6)
Product NDC 60232-2587
Product Type Name HUMAN OTC DRUG
Non Proprietary Name zinc oxide and octinoxate aerosol
Dosage Form Name AEROSOL, SPRAY
Route Name TOPICAL
Start Marketing Date 20120501
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Swiss American Products, Inc.
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 75; 93
Strength Unit g/1000g; g/1000g
Pharmaceutical Classes

Complete Information of Elta MD UV Aero


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