Package 60232-0008-2

Brand: private label super light oil-free spf45

Generic: 2.75% octinsalate, 7.50% octinoxate, 8.00% zinc oxide sunscreen
NDC Package

Package Facts

Identity

Package NDC 60232-0008-2
Digits Only 6023200082
Product NDC 60232-0008
Description

60 g in 1 BOTTLE (60232-0008-2)

Marketing

Marketing Status
Marketed Since 2011-03-22
Brand private label super light oil-free spf45
Generic 2.75% octinsalate, 7.50% octinoxate, 8.00% zinc oxide sunscreen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "c9d33e9b-77bd-4ca7-b228-f49318307a70", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["6a08448a-46bc-4330-ae2d-f716bb4edfa7"], "manufacturer_name": ["Swiss-American CDMO, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 BOTTLE (60232-0008-2)", "package_ndc": "60232-0008-2", "marketing_start_date": "20110322"}], "brand_name": "Private Label Super Light Oil-Free SPF45", "product_id": "60232-0008_c9d33e9b-77bd-4ca7-b228-f49318307a70", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60232-0008", "generic_name": "2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscreen", "labeler_name": "Swiss-American CDMO, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Private Label Super Light Oil-Free SPF45", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 g/1000g"}, {"name": "OCTISALATE", "strength": "27.5 g/1000g"}, {"name": "ZINC OXIDE", "strength": "80 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110322", "listing_expiration_date": "20261231"}