Package 60232-0006-1

Brand: private label spf45 water resistant paraben free sunscreen

Generic: octinoxate, octisalate, zinc oxide sunscreen
NDC Package

Package Facts

Identity

Package NDC 60232-0006-1
Digits Only 6023200061
Product NDC 60232-0006
Description

50 g in 1 BOTTLE (60232-0006-1)

Marketing

Marketing Status
Marketed Since 2011-08-31
Brand private label spf45 water resistant paraben free sunscreen
Generic octinoxate, octisalate, zinc oxide sunscreen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "21e18883-f579-425a-a460-1e601e1b30be", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["f997f4fc-7da5-433c-9a53-2030b489b4f6"], "manufacturer_name": ["Swiss-American CDMO, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (60232-0006-1)", "package_ndc": "60232-0006-1", "marketing_start_date": "20110831"}], "brand_name": "Private Label SPF45 Water Resistant Paraben Free Sunscreen", "product_id": "60232-0006_21e18883-f579-425a-a460-1e601e1b30be", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60232-0006", "generic_name": "Octinoxate, Octisalate, Zinc Oxide Sunscreen", "labeler_name": "Swiss-American CDMO, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Private Label SPF45 Water Resistant Paraben Free Sunscreen", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 g/1000g"}, {"name": "OCTISALATE", "strength": "30 g/1000g"}, {"name": "ZINC OXIDE", "strength": "80 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110831", "listing_expiration_date": "20261231"}