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 |