Package 24330-240-01
Brand: sunburnt plus pain relief
Generic: lidocaine hydrochloridePackage Facts
Identity
Package NDC
24330-240-01
Digits Only
2433024001
Product NDC
24330-240
Description
1 TUBE in 1 CARTON (24330-240-01) / 142 g in 1 TUBE
Marketing
Marketing Status
Brand
sunburnt plus pain relief
Generic
lidocaine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "cd41cc55-ae90-4c02-a405-cc81cd06ce2e", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1012204"], "spl_set_id": ["6363c695-f801-407d-a4e1-b0d9cfa0a273"], "manufacturer_name": ["Welmedix LLC dba Welmedix Consumer Healthcare"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (24330-240-01) / 142 g in 1 TUBE", "package_ndc": "24330-240-01", "marketing_start_date": "20180315"}], "brand_name": "SunBurnt PLUS Pain Relief", "product_id": "24330-240_cd41cc55-ae90-4c02-a405-cc81cd06ce2e", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "24330-240", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Welmedix LLC dba Welmedix Consumer Healthcare", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SunBurnt PLUS Pain Relief", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "part348", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20180315", "listing_expiration_date": "20261231"}