Product NDC: | 62032-125 |
Proprietary Name: | SUN SHIELD BROAD SPECTRUM SPF 50 MATTE |
Non Proprietary Name: | OCTINOXATE and ZINC OXIDE |
Active Ingredient(s): | 75; 105 mg/g; mg/g & nbsp; OCTINOXATE and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62032-125 |
Labeler Name: | OMP, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130221 |
Package NDC: | 62032-125-05 |
Package Description: | 15 g in 1 TUBE (62032-125-05) |
NDC Code | 62032-125-05 |
Proprietary Name | SUN SHIELD BROAD SPECTRUM SPF 50 MATTE |
Package Description | 15 g in 1 TUBE (62032-125-05) |
Product NDC | 62032-125 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130221 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | OMP, Inc. |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 75; 105 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |