Package 56104-502-00

Brand: liquid bandage

Generic: benzethonium chloride plus dyclonine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 56104-502-00
Digits Only 5610450200
Product NDC 56104-502
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-502-00) / 29.6 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2023-09-11
Brand liquid bandage
Generic benzethonium chloride plus dyclonine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4094375b-31ea-3c3a-e063-6294a90ad8f6", "openfda": {"unii": ["PH41D05744", "ZEC193879Q"], "spl_set_id": ["051b68f9-5d6c-3cd7-e063-6394a90aeb35"], "manufacturer_name": ["Premier Brands of America Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-502-00)  / 29.6 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "56104-502-00", "marketing_start_date": "20230911"}], "brand_name": "Liquid Bandage", "product_id": "56104-502_4094375b-31ea-3c3a-e063-6294a90ad8f6", "dosage_form": "LIQUID", "product_ndc": "56104-502", "generic_name": "Benzethonium chloride Plus Dyclonine hydrochloride", "labeler_name": "Premier Brands of America Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Liquid Bandage", "active_ingredients": [{"name": "BENZETHONIUM CHLORIDE", "strength": "2 mg/mL"}, {"name": "DYCLONINE HYDROCHLORIDE", "strength": "7.5 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}