Package 52261-0601-1

Brand: berberex wound gel

Generic: benzethonium chloride, allantoin
NDC Package

Package Facts

Identity

Package NDC 52261-0601-1
Digits Only 5226106011
Product NDC 52261-0601
Product ID 52261-0601_67cabb40-44f2-4ad0-ad14-77f4ab2bd1dc
Description

.085 kg in 1 TUBE (52261-0601-1)

Marketing

Marketing Status
Marketed Since 2022-07-01
Brand berberex wound gel
Generic benzethonium chloride, allantoin
Sample Package No

Linked Drug Pages (1)

Berberex Wound Gel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "67cabb40-44f2-4ad0-ad14-77f4ab2bd1dc", "openfda": {"unii": ["344S277G0Z", "PH41D05744"], "spl_set_id": ["5dd97e65-bfb3-468e-a2b1-e56d30da99df"], "manufacturer_name": ["Cosco International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".085 kg in 1 TUBE (52261-0601-1)", "package_ndc": "52261-0601-1", "marketing_start_date": "20220701"}], "brand_name": "Berberex Wound Gel", "product_id": "52261-0601_67cabb40-44f2-4ad0-ad14-77f4ab2bd1dc", "dosage_form": "GEL", "product_ndc": "52261-0601", "generic_name": "Benzethonium Chloride, Allantoin", "labeler_name": "Cosco International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Berberex Wound Gel", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".005 kg/kg"}, {"name": "BENZETHONIUM CHLORIDE", "strength": ".0012 kg/kg"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220701", "listing_expiration_date": "20261231"}