Kinesys - 61481-0590-2 - (OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE)

Alphabetical Index


Drug Information of Kinesys

Product NDC: 61481-0590
Proprietary Name: Kinesys
Non Proprietary Name: OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE
Active Ingredient(s): 2; 7.5; 4; 7    g/100mL; g/100mL; g/100mL; g/100mL & nbsp;   OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Kinesys

Product NDC: 61481-0590
Labeler Name: KINeSYS Pharmaceutical Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120515

Package Information of Kinesys

Package NDC: 61481-0590-2
Package Description: 30 mL in 1 BOTTLE, SPRAY (61481-0590-2)

NDC Information of Kinesys

NDC Code 61481-0590-2
Proprietary Name Kinesys
Package Description 30 mL in 1 BOTTLE, SPRAY (61481-0590-2)
Product NDC 61481-0590
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20120515
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name KINeSYS Pharmaceutical Inc.
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
Strength Number 2; 7.5; 4; 7
Strength Unit g/100mL; g/100mL; g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of Kinesys


General Information