Product NDC: | 44924-101 |
Proprietary Name: | High Protection Sun SPF 30 |
Non Proprietary Name: | Titanium Dioxide |
Active Ingredient(s): | 15; 15.5 mL/200mL; mL/200mL & nbsp; Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44924-101 |
Labeler Name: | Babor Cosmetics America, Corp. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100301 |
Package NDC: | 44924-101-02 |
Package Description: | 1 TUBE in 1 CARTON (44924-101-02) > 200 mL in 1 TUBE (44924-101-01) |
NDC Code | 44924-101-02 |
Proprietary Name | High Protection Sun SPF 30 |
Package Description | 1 TUBE in 1 CARTON (44924-101-02) > 200 mL in 1 TUBE (44924-101-01) |
Product NDC | 44924-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Babor Cosmetics America, Corp. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 15; 15.5 |
Strength Unit | mL/200mL; mL/200mL |
Pharmaceutical Classes |