Product NDC: | 35192-010 |
Proprietary Name: | Umbrella Sunscreen |
Non Proprietary Name: | Octinoxate Titanium Dioxide |
Active Ingredient(s): | 8.5; 6.8 g/113.4g; g/113.4g & nbsp; Octinoxate Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35192-010 |
Labeler Name: | CA-BOTANA INTERNATIONAL |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120601 |
Package NDC: | 35192-010-02 |
Package Description: | 113.4 g in 1 TUBE (35192-010-02) |
NDC Code | 35192-010-02 |
Proprietary Name | Umbrella Sunscreen |
Package Description | 113.4 g in 1 TUBE (35192-010-02) |
Product NDC | 35192-010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate Titanium Dioxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CA-BOTANA INTERNATIONAL |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 8.5; 6.8 |
Strength Unit | g/113.4g; g/113.4g |
Pharmaceutical Classes |