Package 83324-232-03

Brand: benzethonium chloride and dyclonine hydrochloride

Generic: liquid bandage
NDC Package

Package Facts

Identity

Package NDC 83324-232-03
Digits Only 8332423203
Product NDC 83324-232
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (83324-232-03) / 9 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2025-04-25
Brand benzethonium chloride and dyclonine hydrochloride
Generic liquid bandage
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40969e2f-7ec8-0030-e063-6294a90aa30a", "openfda": {"unii": ["PH41D05744", "ZEC193879Q"], "rxcui": ["1048366"], "spl_set_id": ["34062b23-52aa-99ae-e063-6294a90ae73f"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (83324-232-03)  / 9 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "83324-232-03", "marketing_start_date": "20250425"}], "brand_name": "Benzethonium chloride and Dyclonine hydrochloride", "product_id": "83324-232_40969e2f-7ec8-0030-e063-6294a90aa30a", "dosage_form": "LIQUID", "product_ndc": "83324-232", "generic_name": "Liquid Bandage", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benzethonium chloride and Dyclonine hydrochloride", "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": "20250417", "listing_expiration_date": "20261231"}