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NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50 - 62032-104-90 - (OCTINOXATE and ZINC OXIDE)

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Drug Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50

Product NDC: 62032-104
Proprietary Name: NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50
Non Proprietary Name: OCTINOXATE and ZINC OXIDE
Active Ingredient(s): 75; 105    mg/g; mg/g & nbsp;   OCTINOXATE and ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50

Product NDC: 62032-104
Labeler Name: OMP, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121107

Package Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50

Package NDC: 62032-104-90
Package Description: 85 g in 1 TUBE (62032-104-90)

NDC Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50

NDC Code 62032-104-90
Proprietary Name NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50
Package Description 85 g in 1 TUBE (62032-104-90)
Product NDC 62032-104
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and ZINC OXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20121107
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name OMP, Inc.
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 75; 105
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of NU-DERM SUN SHIELD BROAD SPECTRUM SPF 50


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