Package 24208-001-04

Brand: purpose

Generic: octinoxate, octisalate and oxybenzone
NDC Package

Package Facts

Identity

Package NDC 24208-001-04
Digits Only 2420800104
Product NDC 24208-001
Description

1 BOTTLE in 1 CARTON (24208-001-04) / 113 g in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2013-10-07
Brand purpose
Generic octinoxate, octisalate and oxybenzone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "22f5cdc2-86cc-7dfd-e063-6394a90a539d", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "95OOS7VE0Y"], "spl_set_id": ["a1e14135-b8da-4cee-8c5b-1893572f4de4"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (24208-001-04)  / 113 g in 1 BOTTLE", "package_ndc": "24208-001-04", "marketing_start_date": "20131007"}], "brand_name": "PURPOSE", "product_id": "24208-001_22f5cdc2-86cc-7dfd-e063-6394a90a539d", "dosage_form": "LOTION", "product_ndc": "24208-001", "generic_name": "Octinoxate, Octisalate and Oxybenzone", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PURPOSE", "active_ingredients": [{"name": "OCTINOXATE", "strength": "7.5 g/100g"}, {"name": "OCTISALATE", "strength": "5 g/100g"}, {"name": "OXYBENZONE", "strength": "3 g/100g"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131007", "listing_expiration_date": "20261231"}