Package 70000-0617-1

Brand: leader roll-on cooling pain relief topical analgesic

Generic: menthol, unspecified form
NDC Package

Package Facts

Identity

Package NDC 70000-0617-1
Digits Only 7000006171
Product NDC 70000-0617
Description

74 mL in 1 BOTTLE, WITH APPLICATOR (70000-0617-1)

Marketing

Marketing Status
Marketed Since 2022-11-03
Brand leader roll-on cooling pain relief topical analgesic
Generic menthol, unspecified form
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "f835accf-f50d-4831-b28f-881db7ed2e01", "openfda": {"upc": ["0096295142396"], "unii": ["L7T10EIP3A"], "rxcui": ["415974"], "spl_set_id": ["e86cba40-6b10-454d-98b3-6b547456eaad"], "manufacturer_name": ["Cardinal Health, 110 dba LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74 mL in 1 BOTTLE, WITH APPLICATOR (70000-0617-1)", "package_ndc": "70000-0617-1", "marketing_start_date": "20221103"}], "brand_name": "Leader Roll-On Cooling Pain Relief Topical Analgesic", "product_id": "70000-0617_f835accf-f50d-4831-b28f-881db7ed2e01", "dosage_form": "GEL", "product_ndc": "70000-0617", "generic_name": "MENTHOL, UNSPECIFIED FORM", "labeler_name": "Cardinal Health, 110 dba LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Leader Roll-On Cooling Pain Relief", "brand_name_suffix": "Topical Analgesic", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "40 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221103", "listing_expiration_date": "20261231"}