| 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 |