Product NDC: | 42908-003 |
Proprietary Name: | PAUL and JOE PROTECTIVE FOUNDATION PRIMER UV 02 |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE and ZINC OXIDE |
Active Ingredient(s): | 30; 60; 81 mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42908-003 |
Labeler Name: | Albion Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100301 |
Package NDC: | 42908-003-02 |
Package Description: | 1 TUBE in 1 CARTON (42908-003-02) > 26.9 mL in 1 TUBE |
NDC Code | 42908-003-02 |
Proprietary Name | PAUL and JOE PROTECTIVE FOUNDATION PRIMER UV 02 |
Package Description | 1 TUBE in 1 CARTON (42908-003-02) > 26.9 mL in 1 TUBE |
Product NDC | 42908-003 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE and ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Albion Co., Ltd. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 30; 60; 81 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |