Package 52000-439-25

Brand: 4% menthol pain relief

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 52000-439-25
Digits Only 5200043925
Product NDC 52000-439
Product ID 52000-439_8beb3f46-515f-4b8d-ad05-06be2df6ca08
Description

74 mL in 1 BOTTLE (52000-439-25)

Marketing

Marketing Status
Marketed Since 2026-01-19
Brand 4% menthol pain relief
Generic menthol
Sample Package No

Linked Drug Pages (1)

4% Menthol PAIN RELIEF ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "8beb3f46-515f-4b8d-ad05-06be2df6ca08", "openfda": {"upc": ["0676979560366"], "unii": ["L7T10EIP3A"], "rxcui": ["415974"], "spl_set_id": ["7fb95135-4151-4ef4-bb6d-75251cafff6c"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74 mL in 1 BOTTLE (52000-439-25)", "package_ndc": "52000-439-25", "marketing_start_date": "20260119"}], "brand_name": "4% Menthol PAIN RELIEF", "product_id": "52000-439_8beb3f46-515f-4b8d-ad05-06be2df6ca08", "dosage_form": "GEL", "product_ndc": "52000-439", "generic_name": "Menthol", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "4% Menthol PAIN RELIEF", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "4 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260119", "listing_expiration_date": "20271231"}