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SENSAI
SENSAI - 64159-7046-1 - (OCTINOXATE and TITANIUM DIOXIDE)
Drug Information of SENSAI
| Product NDC: | 64159-7046 |
| 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) |
Labeler Information of SENSAI
| Product NDC: | 64159-7046 |
| Labeler Name: | KANEBO COSMETICS INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100201 |
Package Information of SENSAI
| Package NDC: | 64159-7046-1 |
| Package Description: | 50 mL in 1 TUBE (64159-7046-1) |
NDC Information of SENSAI
| NDC Code | 64159-7046-1 |
| Proprietary Name | SENSAI |
| Package Description | 50 mL in 1 TUBE (64159-7046-1) |
| Product NDC | 64159-7046 |
| 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 |
