| Product NDC: | 42908-052 |
| Proprietary Name: | PAUL and JOE |
| Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
| Active Ingredient(s): | 1.5; 2.94 g/30mL; g/30mL & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42908-052 |
| Labeler Name: | Albion Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110301 |
| Package NDC: | 42908-052-00 |
| Package Description: | 1 BOTTLE, GLASS in 1 BOX (42908-052-00) > 30 mL in 1 BOTTLE, GLASS |
| NDC Code | 42908-052-00 |
| Proprietary Name | PAUL and JOE |
| Package Description | 1 BOTTLE, GLASS in 1 BOX (42908-052-00) > 30 mL in 1 BOTTLE, GLASS |
| Product NDC | 42908-052 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Albion Co., Ltd. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 1.5; 2.94 |
| Strength Unit | g/30mL; g/30mL |
| Pharmaceutical Classes |