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KINESYS
KINESYS - 61481-0045-2 - (OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE)
Drug Information of KINESYS
| Product NDC: | 61481-0045 |
| Proprietary Name: | KINESYS |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.5; 5; 4.5; 1 g/100g; g/100g; g/100g; g/100g & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KINESYS
| Product NDC: | 61481-0045 |
| 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 Information of KINESYS
| Package NDC: | 61481-0045-2 |
| Package Description: | 4 g in 1 TUBE (61481-0045-2) |
NDC Information of KINESYS
| NDC Code | 61481-0045-2 |
| Proprietary Name | KINESYS |
| Package Description | 4 g in 1 TUBE (61481-0045-2) |
| Product NDC | 61481-0045 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20120620 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | KINeSYS Pharmaceutical Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 5; 4.5; 1 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
