JOURNEE - 52318-002-04 - (OCTINOXATE, ZINC OXIDE)

Alphabetical Index


Drug Information of JOURNEE

Product NDC: 52318-002
Proprietary Name: JOURNEE
Non Proprietary Name: OCTINOXATE, ZINC OXIDE
Active Ingredient(s): 75; 73    mg/mL; mg/mL & nbsp;   OCTINOXATE, ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of JOURNEE

Product NDC: 52318-002
Labeler Name: Neocutis, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120618

Package Information of JOURNEE

Package NDC: 52318-002-04
Package Description: 50 mL in 1 BOTTLE (52318-002-04)

NDC Information of JOURNEE

NDC Code 52318-002-04
Proprietary Name JOURNEE
Package Description 50 mL in 1 BOTTLE (52318-002-04)
Product NDC 52318-002
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, ZINC OXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120618
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Neocutis, Inc.
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 75; 73
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of JOURNEE


General Information