Product ID | 60232-0008_1ab1ef26-9f83-40b8-a496-0865b33ed8bd |
NDC | 60232-0008 |
Product Type | Human Otc Drug |
Proprietary Name | Private Label Super Light Oil-Free SPF45 |
Generic Name | 2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscreen |
Dosage Form | Lotion |
Route of Administration | TOPICAL |
Marketing Start Date | 2011-03-22 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part352 |
Labeler Name | Swiss-American CDMO, LLC |
Substance Name | OCTISALATE; OCTINOXATE; ZINC OXIDE |
Active Ingredient Strength | 28 g/1000g; g/1000g; g/1000g |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |