Package 52000-105-01
Brand: universal ice cold analgesic
Generic: mentholPackage Facts
Identity
Package NDC
52000-105-01
Digits Only
5200010501
Product NDC
52000-105
Description
227 g in 1 BOTTLE, PLASTIC (52000-105-01)
Marketing
Marketing Status
Brand
universal ice cold analgesic
Generic
menthol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "58b2217d-5ab4-4db5-8b59-cac4a647b414", "openfda": {"upc": ["0676979248400"], "unii": ["L7T10EIP3A"], "rxcui": ["866128"], "spl_set_id": ["4fdf61d8-a9e0-4cd2-9e3f-0bdedc47a52f"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 BOTTLE, PLASTIC (52000-105-01)", "package_ndc": "52000-105-01", "marketing_start_date": "20200125"}], "brand_name": "Universal Ice Cold Analgesic", "product_id": "52000-105_58b2217d-5ab4-4db5-8b59-cac4a647b414", "dosage_form": "GEL", "product_ndc": "52000-105", "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/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200125", "listing_expiration_date": "20261231"}