Package 70188-006-01

Brand: dermanumb analgesic

Generic: lidocaine hcl
NDC Package

Package Facts

Identity

Package NDC 70188-006-01
Digits Only 7018800601
Product NDC 70188-006
Description

57 g in 1 PACKAGE (70188-006-01)

Marketing

Marketing Status
Marketed Since 2015-07-01
Brand dermanumb analgesic
Generic lidocaine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4357221e-618b-66aa-e063-6394a90a6ccf", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010077", "1747492"], "spl_set_id": ["0ea46890-45c3-4732-bc47-227f7c67daf1"], "manufacturer_name": ["A.T.S. Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "57 g in 1 PACKAGE (70188-006-01)", "package_ndc": "70188-006-01", "marketing_start_date": "20150701"}], "brand_name": "DermaNumb Analgesic", "product_id": "70188-006_4357221e-618b-66aa-e063-6394a90a6ccf", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "70188-006", "generic_name": "Lidocaine HCL", "labeler_name": "A.T.S. Laboratories, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DermaNumb Analgesic", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150701", "listing_expiration_date": "20261231"}