Package 84259-475-00

Brand: sun control broad spectrum spf 30

Generic: homosalate, octisalate, zinc oxide
NDC Package

Package Facts

Identity

Package NDC 84259-475-00
Digits Only 8425947500
Product NDC 84259-475
Description

1 TUBE in 1 BOX (84259-475-00) / 100 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-04-22
Brand sun control broad spectrum spf 30
Generic homosalate, octisalate, zinc oxide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "161fc0cf-491c-2123-e063-6294a90aaa7a", "openfda": {"upc": ["0196852091881"], "unii": ["V06SV4M95S", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["8e34a343-7253-469f-9973-076a7ae26cbc"], "manufacturer_name": ["SKINPLAN.US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (84259-475-00)  / 100 mL in 1 TUBE", "package_ndc": "84259-475-00", "marketing_start_date": "20240422"}], "brand_name": "SUN CONTROL BROAD SPECTRUM SPF 30", "product_id": "84259-475_161fc0cf-491c-2123-e063-6294a90aaa7a", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "84259-475", "generic_name": "HOMOSALATE, OCTISALATE, ZINC OXIDE", "labeler_name": "SKINPLAN.US LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUN CONTROL BROAD SPECTRUM SPF 30", "active_ingredients": [{"name": "HOMOSALATE", "strength": "70 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "ZINC OXIDE", "strength": "60 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240422", "listing_expiration_date": "20261231"}