Package 60232-0006-1
Brand: private label spf45 water resistant paraben free sunscreen
Generic: octinoxate, octisalate, zinc oxide sunscreenPackage 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
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"}