Package 72189-621-35
Brand: lidothol gel
Generic: lidothol gelPackage Facts
Identity
Package NDC
72189-621-35
Digits Only
7218962135
Product NDC
72189-621
Description
1 g in 1 BOX (72189-621-35)
Marketing
Marketing Status
Brand
lidothol gel
Generic
lidothol gel
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["CUTANEOUS"], "spl_id": "34f15ceb-87c2-526d-e063-6294a90a3789", "openfda": {"unii": ["V13007Z41A", "L7T10EIP3A"], "rxcui": ["2257313"], "spl_set_id": ["34f15ceb-87c1-526d-e063-6294a90a3789"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "1 g in 1 BOX (72189-621-35)", "package_ndc": "72189-621-35", "marketing_start_date": "20250512"}], "brand_name": "Lidothol Gel", "product_id": "72189-621_34f15ceb-87c2-526d-e063-6294a90a3789", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "72189-621", "generic_name": "Lidothol Gel", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidothol Gel", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "4.5 g/100g"}, {"name": "MENTHOL", "strength": "5 g/100g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250512", "listing_expiration_date": "20261231"}