Package 73240-904-01

Brand: sunmed pain freeze

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 73240-904-01
Digits Only 7324090401
Product NDC 73240-904
Description

89 mL in 1 BOTTLE, PLASTIC (73240-904-01)

Marketing

Marketing Status
Marketed Since 2025-08-19
Brand sunmed pain freeze
Generic menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3cbd785f-2ab1-56e2-e063-6294a90a65fc", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["ff49699c-ced9-13d2-e053-6394a90af079"], "manufacturer_name": ["Sunflora Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89 mL in 1 BOTTLE, PLASTIC (73240-904-01)", "package_ndc": "73240-904-01", "marketing_start_date": "20250819"}], "brand_name": "SUNMED pain freeze", "product_id": "73240-904_3cbd785f-2ab1-56e2-e063-6294a90a65fc", "dosage_form": "SPRAY", "product_ndc": "73240-904", "generic_name": "MENTHOL", "labeler_name": "Sunflora Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUNMED pain freeze", "active_ingredients": [{"name": "MENTHOL", "strength": "6 g/100mL"}], "application_number": "M017.10", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250819", "listing_expiration_date": "20261231"}