Package 85431-202-50

Brand: mineral sunscreen dry touch nt

Generic: titanium dioxide, zinc oxide
NDC Package

Package Facts

Identity

Package NDC 85431-202-50
Digits Only 8543120250
Product NDC 85431-202
Description

53 g in 1 BOTTLE, PUMP (85431-202-50)

Marketing

Marketing Status
Marketed Since 2022-10-28
Brand mineral sunscreen dry touch nt
Generic titanium dioxide, zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "458708b4-56b7-8d18-e063-6294a90a8c47", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["334ffc49-3196-0995-e063-6394a90ad559"], "manufacturer_name": ["Cutis Wellness Dermatology And Dermatopathology PLLC"]}, "finished": true, "packaging": [{"sample": false, "description": "53 g in 1 BOTTLE, PUMP (85431-202-50)", "package_ndc": "85431-202-50", "marketing_start_date": "20221028"}], "brand_name": "Mineral Sunscreen Dry Touch NT", "product_id": "85431-202_458708b4-56b7-8d18-e063-6294a90a8c47", "dosage_form": "CREAM", "product_ndc": "85431-202", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "Cutis Wellness Dermatology And Dermatopathology PLLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mineral Sunscreen Dry Touch NT", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "80 mg/g"}, {"name": "ZINC OXIDE", "strength": "38 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221028", "listing_expiration_date": "20261231"}