Package 51452-037-06
Brand: point relief cold spot pain relieving roll-on
Generic: mentholPackage Facts
Identity
Package NDC
51452-037-06
Digits Only
5145203706
Product NDC
51452-037
Description
90 mL in 1 CONTAINER (51452-037-06)
Marketing
Marketing Status
Brand
point relief cold spot pain relieving roll-on
Generic
menthol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0973b73d-5dde-0986-e063-6294a90a5917", "openfda": {"upc": ["0714905024701"], "unii": ["L7T10EIP3A"], "rxcui": ["2121681", "2121685"], "spl_set_id": ["3f1db0ad-aaa8-4e14-9349-45057e0fb4a6"], "manufacturer_name": ["Fabrication Enterprises"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 CONTAINER (51452-037-06)", "package_ndc": "51452-037-06", "marketing_start_date": "20190401"}], "brand_name": "Point Relief cold Spot Pain Relieving roll-on", "product_id": "51452-037_0973b73d-5dde-0986-e063-6294a90a5917", "dosage_form": "LIQUID", "product_ndc": "51452-037", "generic_name": "MENTHOL", "labeler_name": "Fabrication Enterprises", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Point Relief cold Spot Pain Relieving roll-on", "active_ingredients": [{"name": "MENTHOL", "strength": "140 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}