Package 82240-619-00

Brand: dermaka sunscreen spf 42, tinted

Generic: titanium dioxide, zinc oxide
NDC Package

Package Facts

Identity

Package NDC 82240-619-00
Digits Only 8224061900
Product NDC 82240-619
Description

5 mL in 1 PACKET (82240-619-00)

Marketing

Marketing Status
Marketed Since 2025-06-03
Brand dermaka sunscreen spf 42, tinted
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": "37b123bf-b595-e935-e063-6394a90a6dd0", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["9a967cd1-9eec-4255-b14b-ac2e33e4dbf0"], "manufacturer_name": ["DERMAKA SKIN PRODUCTS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 PACKET (82240-619-00)", "package_ndc": "82240-619-00", "marketing_start_date": "20250603"}], "brand_name": "Dermaka Sunscreen SPF 42, Tinted", "product_id": "82240-619_37b123bf-b595-e935-e063-6394a90a6dd0", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "82240-619", "generic_name": "TITANIUM DIOXIDE, ZINC OXIDE", "labeler_name": "DERMAKA SKIN PRODUCTS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dermaka Sunscreen SPF 42, Tinted", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "60 mg/mL"}, {"name": "ZINC OXIDE", "strength": "77 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250603", "listing_expiration_date": "20261231"}