Package 72188-170-03

Brand: maxocaine pain relieving roll-on

Generic: lidocaine hydrochloride, menthol
NDC Package

Package Facts

Identity

Package NDC 72188-170-03
Digits Only 7218817003
Product NDC 72188-170
Description

88 mL in 1 BOTTLE, WITH APPLICATOR (72188-170-03)

Marketing

Marketing Status
Marketed Since 2018-03-01
Brand maxocaine pain relieving roll-on
Generic lidocaine hydrochloride, menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09dc681e-2348-4213-e063-6394a90a41e1", "openfda": {"upc": ["0787639610960"], "unii": ["V13007Z41A", "L7T10EIP3A"], "rxcui": ["2002008"], "spl_set_id": ["c263d5f2-89b9-4dfd-91c8-f894e5f956c9"], "manufacturer_name": ["Prime Commerce, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE, WITH APPLICATOR (72188-170-03)", "package_ndc": "72188-170-03", "marketing_start_date": "20180301"}], "brand_name": "MAXOCAINE PAIN RELIEVING ROLL-ON", "product_id": "72188-170_09dc681e-2348-4213-e063-6394a90a41e1", "dosage_form": "LIQUID", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "72188-170", "generic_name": "LIDOCAINE HYDROCHLORIDE, MENTHOL", "labeler_name": "Prime Commerce, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXOCAINE PAIN RELIEVING ROLL-ON", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}, {"name": "MENTHOL", "strength": "10 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180301", "listing_expiration_date": "20261231"}