Package 51452-035-02

Brand: point relief cold spot pain relieving

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 51452-035-02
Digits Only 5145203502
Product NDC 51452-035
Description

475 mL in 1 BOTTLE (51452-035-02)

Marketing

Marketing Status
Marketed Since 2019-04-01
Brand point relief cold spot pain relieving
Generic menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0fc4ec9e-6c21-5a8c-e063-6394a90a11ef", "openfda": {"upc": ["0714905025104", "0714905025074", "0714905024305", "0714905031105", "0714905024596"], "unii": ["L7T10EIP3A"], "rxcui": ["2121666"], "spl_set_id": ["ad5d6f04-15e6-4548-95c2-32271c186bc1"], "manufacturer_name": ["Fabrication Enterprises"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "475 mL in 1 BOTTLE (51452-035-02)", "package_ndc": "51452-035-02", "marketing_start_date": "20190401"}, {"sample": false, "description": "3800 mL in 1 JUG (51452-035-03)", "package_ndc": "51452-035-03", "marketing_start_date": "20190401"}, {"sample": false, "description": "950 mL in 1 BOTTLE (51452-035-05)", "package_ndc": "51452-035-05", "marketing_start_date": "20190401"}], "brand_name": "Point Relief Cold Spot Pain Relieving", "product_id": "51452-035_0fc4ec9e-6c21-5a8c-e063-6394a90a11ef", "dosage_form": "GEL", "product_ndc": "51452-035", "generic_name": "MENTHOL", "labeler_name": "Fabrication Enterprises", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Point Relief Cold Spot Pain Relieving", "active_ingredients": [{"name": "MENTHOL", "strength": "120 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}