Package 83083-002-50

Brand: activated mineral sunscreen tinted

Generic: activated mineral sunscreen tinted
NDC Package

Package 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
Marketed Since 2025-03-25
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"}