IOPE SS - 43419-359-06 - (Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE)

Alphabetical Index


Drug Information of IOPE SS

Product NDC: 43419-359
Proprietary Name: IOPE SS
Non Proprietary Name: Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE
Active Ingredient(s): .05; .03; .01    mL/mL; mL/mL; mL/mL & nbsp;   Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of IOPE SS

Product NDC: 43419-359
Labeler Name: AMOREPACIFIC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101101

Package Information of IOPE SS

Package NDC: 43419-359-06
Package Description: 35 mL in 1 BOTTLE (43419-359-06)

NDC Information of IOPE SS

NDC Code 43419-359-06
Proprietary Name IOPE SS
Package Description 35 mL in 1 BOTTLE (43419-359-06)
Product NDC 43419-359
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20101101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AMOREPACIFIC
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number .05; .03; .01
Strength Unit mL/mL; mL/mL; mL/mL
Pharmaceutical Classes

Complete Information of IOPE SS


General Information