Package 47593-670-59

Brand: kay foaming hand sanitizer

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 47593-670-59
Digits Only 4759367059
Product NDC 47593-670
Product ID 47593-670_b2264c8c-11ca-4017-aa68-83a06714ea93
Description

1250 mL in 1 BOTTLE, PLASTIC (47593-670-59)

Marketing

Marketing Status
Marketed Since 2025-12-17
Brand kay foaming hand sanitizer
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Kay Foaming Hand Sanitizer ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "b2264c8c-11ca-4017-aa68-83a06714ea93", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1038799"], "spl_set_id": ["f71032b9-9c7e-458f-8859-4548dfd86217"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1250 mL in 1 BOTTLE, PLASTIC (47593-670-59)", "package_ndc": "47593-670-59", "marketing_start_date": "20251217"}], "brand_name": "Kay Foaming Hand Sanitizer", "product_id": "47593-670_b2264c8c-11ca-4017-aa68-83a06714ea93", "dosage_form": "SOLUTION", "product_ndc": "47593-670", "generic_name": "Benzalkonium Chloride", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kay Foaming Hand Sanitizer", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251217", "listing_expiration_date": "20261231"}