Package 58411-124-30

Brand: shiseido uv protective compact (refill) light ochre

Generic: octinoxate, octocrylene, and titanium dioxide
NDC Package

Package Facts

Identity

Package NDC 58411-124-30
Digits Only 5841112430
Product NDC 58411-124
Description

1 TRAY in 1 CARTON (58411-124-30) / 12 g in 1 TRAY

Marketing

Marketing Status
Marketed Since 2014-02-01
Brand shiseido uv protective compact (refill) light ochre
Generic octinoxate, octocrylene, and titanium dioxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4ba6bd60-913b-4748-e063-6394a90aed10", "openfda": {"unii": ["4Y5P7MUD51", "15FIX9V2JP", "5A68WGF6WM"], "spl_set_id": ["c05cef12-a6a7-4682-9357-6d77f4ca3267"], "manufacturer_name": ["SHISEIDO AMERICAS CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TRAY in 1 CARTON (58411-124-30)  / 12 g in 1 TRAY", "package_ndc": "58411-124-30", "marketing_start_date": "20140201"}], "brand_name": "SHISEIDO UV PROTECTIVE COMPACT (REFILL) LIGHT OCHRE", "product_id": "58411-124_4ba6bd60-913b-4748-e063-6394a90aed10", "dosage_form": "POWDER", "product_ndc": "58411-124", "generic_name": "OCTINOXATE, OCTOCRYLENE, and TITANIUM DIOXIDE", "labeler_name": "SHISEIDO AMERICAS CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SHISEIDO UV PROTECTIVE COMPACT (REFILL)", "brand_name_suffix": "LIGHT OCHRE", "active_ingredients": [{"name": "OCTINOXATE", "strength": "888 mg/12g"}, {"name": "OCTOCRYLENE", "strength": "600 mg/12g"}, {"name": "TITANIUM DIOXIDE", "strength": "1416 mg/12g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140201", "listing_expiration_date": "20271231"}