Package 85373-208-50
Brand: parasol daily mineral sunscreen
Generic: zinc oxidePackage Facts
Identity
Package NDC
85373-208-50
Digits Only
8537320850
Product NDC
85373-208
Description
50 g in 1 BOTTLE, PUMP (85373-208-50)
Marketing
Marketing Status
Brand
parasol daily mineral sunscreen
Generic
zinc oxide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "46044770-a650-78d2-e063-6294a90afbc4", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["35d2fbeb-935b-f0a9-e063-6294a90acd79"], "manufacturer_name": ["Bodi & Wax, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE, PUMP (85373-208-50)", "package_ndc": "85373-208-50", "marketing_start_date": "20250505"}], "brand_name": "Parasol Daily Mineral Sunscreen", "product_id": "85373-208_46044770-a650-78d2-e063-6294a90afbc4", "dosage_form": "CREAM", "product_ndc": "85373-208", "generic_name": "Zinc Oxide", "labeler_name": "Bodi & Wax, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Parasol Daily Mineral Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250505", "listing_expiration_date": "20261231"}