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) |
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 NDC: | 61481-0045-3 |
Package Description: | 1 TUBE in 1 PACKAGE (61481-0045-3) > 7.3 g in 1 TUBE (61481-0045-1) |
NDC Code | 61481-0045-3 |
Proprietary Name | KINESYS |
Package Description | 1 TUBE in 1 PACKAGE (61481-0045-3) > 7.3 g in 1 TUBE (61481-0045-1) |
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 |