Package 10742-8573-1

Brand: softlips pearl

Generic: octinoxate, octisalate
NDC Package

Package Facts

Identity

Package NDC 10742-8573-1
Digits Only 1074285731
Product NDC 10742-8573
Description

1 TUBE in 1 BLISTER PACK (10742-8573-1) / 2 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2010-02-01
Brand softlips pearl
Generic octinoxate, octisalate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2979d20c-f978-246c-e063-6294a90a2df5", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W"], "spl_set_id": ["43e175b4-7a48-431e-bf27-9ce7dee53f5e"], "manufacturer_name": ["The Mentholatum Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BLISTER PACK (10742-8573-1)  / 2 g in 1 TUBE", "package_ndc": "10742-8573-1", "marketing_start_date": "20100201"}], "brand_name": "Softlips Pearl", "product_id": "10742-8573_2979d20c-f978-246c-e063-6294a90a2df5", "dosage_form": "STICK", "product_ndc": "10742-8573", "generic_name": "octinoxate, octisalate", "labeler_name": "The Mentholatum Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Softlips Pearl", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 mg/g"}, {"name": "OCTISALATE", "strength": "50 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100201", "listing_expiration_date": "20261231"}