Natria - 44717-533-02 - (Ethylhexyl Methoxycinnamate, Zinc Oxide)

Alphabetical Index


Drug Information of Natria

Product NDC: 44717-533
Proprietary Name: Natria
Non Proprietary Name: Ethylhexyl Methoxycinnamate, Zinc Oxide
Active Ingredient(s): 7.5; 2.5    mL/100mL; mL/100mL & nbsp;   Ethylhexyl Methoxycinnamate, Zinc Oxide
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Natria

Product NDC: 44717-533
Labeler Name: Wasatch Product Development
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100101

Package Information of Natria

Package NDC: 44717-533-02
Package Description: 1 TUBE in 1 BOX (44717-533-02) > 75 mL in 1 TUBE (44717-533-01)

NDC Information of Natria

NDC Code 44717-533-02
Proprietary Name Natria
Package Description 1 TUBE in 1 BOX (44717-533-02) > 75 mL in 1 TUBE (44717-533-01)
Product NDC 44717-533
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethylhexyl Methoxycinnamate, Zinc Oxide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Wasatch Product Development
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 7.5; 2.5
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Natria


General Information