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Kinesys
Kinesys - 61481-3004-4 - (OCTINOXATE, OCTOCRYLENE, OCTISALATE, and Avobenzone)
Drug Information of Kinesys
| Product NDC: | 61481-3004 |
| Proprietary Name: | Kinesys |
| Non Proprietary Name: | OCTINOXATE, OCTOCRYLENE, OCTISALATE, and Avobenzone |
| Active Ingredient(s): | 2.5; 7.5; 5; 7.5 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: | 61481-3004 |
| Labeler Name: | KINeSYS Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130304 |
Package Information of Kinesys
| Package NDC: | 61481-3004-4 |
| Package Description: | 120 mL in 1 BOTTLE, SPRAY (61481-3004-4) |
NDC Information of Kinesys
| NDC Code | 61481-3004-4 |
| Proprietary Name | Kinesys |
| Package Description | 120 mL in 1 BOTTLE, SPRAY (61481-3004-4) |
| Product NDC | 61481-3004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTOCRYLENE, OCTISALATE, and Avobenzone |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130304 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | KINeSYS Pharmaceuticals Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 2.5; 7.5; 5; 7.5 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
