Package 67234-008-01

Brand: anti itch maximum relief

Generic: pramoxine hydrochloride and menthol
NDC Package

Package Facts

Identity

Package NDC 67234-008-01
Digits Only 6723400801
Product NDC 67234-008
Description

1 TUBE in 1 BOX (67234-008-01) / 42 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2008-01-02
Brand anti itch maximum relief
Generic pramoxine hydrochloride and menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "eba79205-9b9e-495e-a57c-c1d980a90e22", "openfda": {"unii": ["L7T10EIP3A", "88AYB867L5"], "rxcui": ["1116155"], "spl_set_id": ["75de3d5e-ecbe-4d04-a39d-792200e6ee32"], "manufacturer_name": ["Natureplex LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (67234-008-01)  / 42 g in 1 TUBE", "package_ndc": "67234-008-01", "marketing_start_date": "20080102"}], "brand_name": "Anti Itch Maximum Relief", "product_id": "67234-008_eba79205-9b9e-495e-a57c-c1d980a90e22", "dosage_form": "CREAM", "product_ndc": "67234-008", "generic_name": "Pramoxine Hydrochloride and Menthol", "labeler_name": "Natureplex LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti Itch", "brand_name_suffix": "Maximum Relief", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "10 mg/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080102", "listing_expiration_date": "20261231"}