Package 52000-106-01

Brand: universal ice cold analgesic

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 52000-106-01
Digits Only 5200010601
Product NDC 52000-106
Product ID 52000-106_b89ff727-4759-4299-ae51-29faad8a69dd
Description

237 mL in 1 TUBE (52000-106-01)

Marketing

Marketing Status
Marketed Since 2020-05-01
Brand universal ice cold analgesic
Generic menthol
Sample Package No

Linked Drug Pages (1)

Universal Ice Cold Analgesic ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "b89ff727-4759-4299-ae51-29faad8a69dd", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["866128"], "spl_set_id": ["79ad55eb-b59d-4bb8-88e3-3b51e10a7f28"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 TUBE (52000-106-01)", "package_ndc": "52000-106-01", "marketing_start_date": "20200501"}], "brand_name": "Universal Ice Cold Analgesic", "product_id": "52000-106_b89ff727-4759-4299-ae51-29faad8a69dd", "dosage_form": "GEL", "product_ndc": "52000-106", "generic_name": "Menthol", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Universal Ice Cold Analgesic", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "1.25 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}