Home > National Drug Code (NDC) > ISA KNOX 365 SUN

ISA KNOX 365 SUN - 53208-502-02 - (ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE)

Alphabetical Index


Drug Information of ISA KNOX 365 SUN

Product NDC: 53208-502
Proprietary Name: ISA KNOX 365 SUN
Non Proprietary Name: ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE
Active Ingredient(s): 7.2; 4.03; 11.04    mL/100mL; mL/100mL; mL/100mL & nbsp;   ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ISA KNOX 365 SUN

Product NDC: 53208-502
Labeler Name: LG Household and Healthcare, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100330

Package Information of ISA KNOX 365 SUN

Package NDC: 53208-502-02
Package Description: 1 CONTAINER in 1 BOX (53208-502-02) > 70 mL in 1 CONTAINER (53208-502-01)

NDC Information of ISA KNOX 365 SUN

NDC Code 53208-502-02
Proprietary Name ISA KNOX 365 SUN
Package Description 1 CONTAINER in 1 BOX (53208-502-02) > 70 mL in 1 CONTAINER (53208-502-01)
Product NDC 53208-502
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100330
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name LG Household and Healthcare, Inc.
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 7.2; 4.03; 11.04
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of ISA KNOX 365 SUN


General Information