Package 51042-001-10

Brand: first mark ultra foaming antibacterial

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 51042-001-10
Digits Only 5104200110
Product NDC 51042-001
Product ID 51042-001_f855444d-b8b3-4200-8ebe-481bb30ee25f
Description

1250 mL in 1 BOTTLE (51042-001-10)

Marketing

Marketing Status
Marketed Since 2021-11-29
Brand first mark ultra foaming antibacterial
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

FIRST MARK ULTRA FOAMING ANTIBACTERIAL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "f855444d-b8b3-4200-8ebe-481bb30ee25f", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["968c0f18-d0b6-4f29-b001-00ac314a3bdd"], "manufacturer_name": ["Performance Food Group"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1250 mL in 1 BOTTLE (51042-001-10)", "package_ndc": "51042-001-10", "marketing_start_date": "20211129"}], "brand_name": "FIRST MARK ULTRA FOAMING ANTIBACTERIAL", "product_id": "51042-001_f855444d-b8b3-4200-8ebe-481bb30ee25f", "dosage_form": "SOLUTION", "product_ndc": "51042-001", "generic_name": "Benzalkonium Chloride", "labeler_name": "Performance Food Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FIRST MARK ULTRA FOAMING ANTIBACTERIAL", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "5 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150812", "listing_expiration_date": "20261231"}