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KINESYS
KINESYS - 61481-0450-2 - (OCTINOXATE, OCTISALATE, and AVOBENZONE)
Drug Information of KINESYS
| Product NDC: | 61481-0450 |
| Proprietary Name: | KINESYS |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, and AVOBENZONE |
| Active Ingredient(s): | 2; 7.5; 5 g/100mL; g/100mL; g/100mL & nbsp; OCTINOXATE, OCTISALATE, and AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KINESYS
| Product NDC: | 61481-0450 |
| Labeler Name: | KINeSYS Pharmaceutical Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120530 |
Package Information of KINESYS
| Package NDC: | 61481-0450-2 |
| Package Description: | 30 mL in 1 BOTTLE, SPRAY (61481-0450-2) |
NDC Information of KINESYS
| NDC Code | 61481-0450-2 |
| Proprietary Name | KINESYS |
| Package Description | 30 mL in 1 BOTTLE, SPRAY (61481-0450-2) |
| Product NDC | 61481-0450 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, and AVOBENZONE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120530 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | KINeSYS Pharmaceutical Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 2; 7.5; 5 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
