| 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 |