Package 85431-226-50
Brand: mineral sunscreen moisturizing non-tinted
Generic: zinc oxidePackage Facts
Identity
Package NDC
85431-226-50
Digits Only
8543122650
Product NDC
85431-226
Description
50 g in 1 BOTTLE, PUMP (85431-226-50)
Marketing
Marketing Status
Brand
mineral sunscreen moisturizing non-tinted
Generic
zinc oxide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45870e47-7775-4eb8-e063-6394a90a7ec3", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["3360a208-5f17-a74b-e063-6294a90a13e1"], "manufacturer_name": ["Cutis Wellness Dermatology And Dermatopathology PLLC"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE, PUMP (85431-226-50)", "package_ndc": "85431-226-50", "marketing_start_date": "20230120"}], "brand_name": "Mineral Sunscreen Moisturizing Non-Tinted", "product_id": "85431-226_45870e47-7775-4eb8-e063-6394a90a7ec3", "dosage_form": "CREAM", "product_ndc": "85431-226", "generic_name": "Zinc Oxide", "labeler_name": "Cutis Wellness Dermatology And Dermatopathology PLLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mineral Sunscreen Moisturizing Non-Tinted", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230120", "listing_expiration_date": "20261231"}