Product NDC: | 64159-7047 |
Proprietary Name: | SENSAI |
Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
Active Ingredient(s): | 3.5; .89 g/100mL; g/100mL & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64159-7047 |
Labeler Name: | KANEBO COSMETICS INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100201 |
Package NDC: | 64159-7047-1 |
Package Description: | 50 mL in 1 TUBE (64159-7047-1) |
NDC Code | 64159-7047-1 |
Proprietary Name | SENSAI |
Package Description | 50 mL in 1 TUBE (64159-7047-1) |
Product NDC | 64159-7047 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | KANEBO COSMETICS INC. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 3.5; .89 |
Strength Unit | g/100mL; g/100mL |
Pharmaceutical Classes |