Package 85431-202-50
Brand: mineral sunscreen dry touch nt
Generic: titanium dioxide, zinc oxidePackage 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
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"}