Package 82442-019-01

Brand: benzethonium chloride and dyclonine hydrochloride

Generic: liquid bandage
NDC Package

Package Facts

Identity

Package NDC 82442-019-01
Digits Only 8244201901
Product NDC 82442-019
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (82442-019-01) / 29.6 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2025-04-09
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": "40969373-1d8d-d8ea-e063-6294a90aaca1", "openfda": {"upc": ["0034197015394"], "unii": ["PH41D05744", "ZEC193879Q"], "rxcui": ["1048366"], "spl_set_id": ["326daa64-165a-cea6-e063-6294a90afbab"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (82442-019-01)  / 29.6 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "82442-019-01", "marketing_start_date": "20250409"}], "brand_name": "Benzethonium chloride and Dyclonine hydrochloride", "product_id": "82442-019_40969373-1d8d-d8ea-e063-6294a90aaca1", "dosage_form": "LIQUID", "product_ndc": "82442-019", "generic_name": "Liquid Bandage", "labeler_name": "Target Corporation", "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": "20250409", "listing_expiration_date": "20261231"}