Package 50390-111-00

Brand: artistry youth xtend lifting smoothing foundation broad spectrum spf 20 sunscreen

Generic: octinoxate, oxybenzone
NDC Package

Package Facts

Identity

Package NDC 50390-111-00
Digits Only 5039011100
Product NDC 50390-111
Product ID 50390-111_083830bb-0805-7b2c-e063-6394a90abfbe
Description

30 mL in 1 BOTTLE (50390-111-00)

Marketing

Marketing Status
Marketed Since 2013-05-06
Brand artistry youth xtend lifting smoothing foundation broad spectrum spf 20 sunscreen
Generic octinoxate, oxybenzone
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "083830bb-0805-7b2c-e063-6394a90abfbe", "openfda": {"unii": ["4Y5P7MUD51", "95OOS7VE0Y"], "spl_set_id": ["8cde14ae-b886-4bd2-b2bd-db604373984a"], "manufacturer_name": ["Amway Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (50390-111-00)", "package_ndc": "50390-111-00", "marketing_start_date": "20130506"}], "brand_name": "ARTISTRY YOUTH XTEND Lifting Smoothing Foundation Broad Spectrum SPF 20 Sunscreen", "product_id": "50390-111_083830bb-0805-7b2c-e063-6394a90abfbe", "dosage_form": "CREAM", "product_ndc": "50390-111", "generic_name": "OCTINOXATE, OXYBENZONE", "labeler_name": "Amway Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ARTISTRY YOUTH XTEND Lifting Smoothing Foundation Broad Spectrum SPF 20 Sunscreen", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 mg/mL"}, {"name": "OXYBENZONE", "strength": "5 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130506", "listing_expiration_date": "20261231"}