Package 51452-036-06
Brand: point relief cold spot pain relieving
Generic: mentholPackage Facts
Identity
Package NDC
51452-036-06
Digits Only
5145203606
Product NDC
51452-036
Description
5 g in 1 PACKET (51452-036-06)
Marketing
Marketing Status
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": "0973ce0d-48e1-5977-e063-6394a90ad88e", "openfda": {"upc": ["0714905024732"], "unii": ["L7T10EIP3A"], "rxcui": ["2121666", "2121669"], "spl_set_id": ["391af69f-74aa-48cf-bc96-75e5c4e0e445"], "manufacturer_name": ["Fabrication Enterprises"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 g in 1 PACKET (51452-036-06)", "package_ndc": "51452-036-06", "marketing_start_date": "20190401"}], "brand_name": "Point Relief Cold Spot Pain Relieving", "product_id": "51452-036_0973ce0d-48e1-5977-e063-6394a90ad88e", "dosage_form": "GEL", "product_ndc": "51452-036", "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/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}