Package 83083-002-50
Brand: activated mineral sunscreen tinted
Generic: activated mineral sunscreen tintedPackage Facts
Identity
Package NDC
83083-002-50
Digits Only
8308300250
Product NDC
83083-002
Description
1 TUBE in 1 CARTON (83083-002-50) / 50 mL in 1 TUBE
Marketing
Marketing Status
Brand
activated mineral sunscreen tinted
Generic
activated mineral sunscreen tinted
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "452053bf-8b70-6550-e063-6294a90a23be", "openfda": {"upc": ["0198168599846"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["312a32a7-d253-f10c-e063-6294a90a803a"], "manufacturer_name": ["Reve Skincare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (83083-002-50) / 50 mL in 1 TUBE", "package_ndc": "83083-002-50", "marketing_start_date": "20250325"}], "brand_name": "Activated Mineral Sunscreen Tinted", "product_id": "83083-002_452053bf-8b70-6550-e063-6294a90a23be", "dosage_form": "CREAM", "product_ndc": "83083-002", "generic_name": "Activated Mineral Sunscreen Tinted", "labeler_name": "Reve Skincare LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Activated Mineral Sunscreen Tinted", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "142.8 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250325", "listing_expiration_date": "20261231"}