Package 82617-103-59

Brand: black label b numb

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82617-103-59
Digits Only 8261710359
Product NDC 82617-103
Description

59 mL in 1 BOTTLE, SPRAY (82617-103-59)

Marketing

Marketing Status
Marketed Since 2024-02-22
Brand black label b numb
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "47f815d3-5090-241d-e063-6294a90a802a", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["2624687"], "spl_set_id": ["11fcf401-0891-04bc-e063-6294a90a8ad5"], "manufacturer_name": ["SCALP TECH INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, SPRAY (82617-103-59)", "package_ndc": "82617-103-59", "marketing_start_date": "20240222"}], "brand_name": "BLACK LABEL B NUMB", "product_id": "82617-103_47f815d3-5090-241d-e063-6294a90a802a", "dosage_form": "SPRAY", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "82617-103", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "SCALP TECH INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BLACK LABEL", "brand_name_suffix": "B NUMB", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "5 g/100mL"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230223", "listing_expiration_date": "20271231"}