Product NDC: | 61481-0680 |
Proprietary Name: | KINESYS |
Non Proprietary Name: | HOMOSALATE, OXYBENZONE, OCTISALATE, and AVOBENZONE |
Active Ingredient(s): | 3; 15; 5; 6 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; HOMOSALATE, OXYBENZONE, OCTISALATE, and AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61481-0680 |
Labeler Name: | KINeSYS Pharmaceutical Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120620 |
Package NDC: | 61481-0680-3 |
Package Description: | 2 BOTTLE, SPRAY in 1 PACKAGE, COMBINATION (61481-0680-3) > 120 mL in 1 BOTTLE, SPRAY (61481-0680-1) |
NDC Code | 61481-0680-3 |
Proprietary Name | KINESYS |
Package Description | 2 BOTTLE, SPRAY in 1 PACKAGE, COMBINATION (61481-0680-3) > 120 mL in 1 BOTTLE, SPRAY (61481-0680-1) |
Product NDC | 61481-0680 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HOMOSALATE, OXYBENZONE, OCTISALATE, and AVOBENZONE |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20120620 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | KINeSYS Pharmaceutical Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
Strength Number | 3; 15; 5; 6 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |