Package 60232-0007-1

Brand: private label moisturizing oil free paraben free spf43

Generic: sunscreen
NDC Package

Package Facts

Identity

Package NDC 60232-0007-1
Digits Only 6023200071
Product NDC 60232-0007
Description

50 g in 1 BOTTLE (60232-0007-1)

Marketing

Marketing Status
Marketed Since 2010-05-07
Brand private label moisturizing oil free paraben free spf43
Generic sunscreen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4e399a9d-b92c-4483-962a-4d65f8cddc30", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["003e4221-f9d9-47c4-b10b-9876046b931a"], "manufacturer_name": ["Swiss-American CDMO, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (60232-0007-1)", "package_ndc": "60232-0007-1", "marketing_start_date": "20100507"}], "brand_name": "Private Label Moisturizing Oil Free Paraben Free SPF43", "product_id": "60232-0007_4e399a9d-b92c-4483-962a-4d65f8cddc30", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60232-0007", "generic_name": "Sunscreen", "labeler_name": "Swiss-American CDMO, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Private Label Moisturizing Oil Free Paraben Free SPF43", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 g/1000g"}, {"name": "OCTISALATE", "strength": "25 g/1000g"}, {"name": "ZINC OXIDE", "strength": "75 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100507", "listing_expiration_date": "20261231"}