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EltaMD UV Facial - 60232-2283-3 - (Zinc Oxide, Octinoxate)

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Drug Information of EltaMD UV Facial

Product NDC: 60232-2283
Proprietary Name: EltaMD UV Facial
Non Proprietary Name: Zinc Oxide, Octinoxate
Active Ingredient(s): 75; 70    g/1000g; g/1000g & nbsp;   Zinc Oxide, Octinoxate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of EltaMD UV Facial

Product NDC: 60232-2283
Labeler Name: Swiss-American Products
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20020430

Package Information of EltaMD UV Facial

Package NDC: 60232-2283-3
Package Description: 86 g in 1 TUBE (60232-2283-3)

NDC Information of EltaMD UV Facial

NDC Code 60232-2283-3
Proprietary Name EltaMD UV Facial
Package Description 86 g in 1 TUBE (60232-2283-3)
Product NDC 60232-2283
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Zinc Oxide, Octinoxate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20020430
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Swiss-American Products
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 75; 70
Strength Unit g/1000g; g/1000g
Pharmaceutical Classes

Complete Information of EltaMD UV Facial


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