Package 21749-610-40

Brand: purell antimicrobial foaming hand

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 21749-610-40
Digits Only 2174961040
Product NDC 21749-610
Product ID 21749-610_2a976ebe-2fd0-a496-e063-6294a90a2dae
Description

1200 mL in 1 PACKAGE (21749-610-40)

Marketing

Marketing Status
Marketed Since 2023-12-11
Brand purell antimicrobial foaming hand
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

PURELL Antimicrobial Foaming Hand ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2a976ebe-2fd0-a496-e063-6294a90a2dae", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["fd5d9942-1cd3-4c40-84bf-beb432768219"], "manufacturer_name": ["GOJO Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1200 mL in 1 PACKAGE (21749-610-40)", "package_ndc": "21749-610-40", "marketing_start_date": "20231211"}], "brand_name": "PURELL Antimicrobial Foaming Hand", "product_id": "21749-610_2a976ebe-2fd0-a496-e063-6294a90a2dae", "dosage_form": "LIQUID", "product_ndc": "21749-610", "generic_name": "Benzalkonium Chloride", "labeler_name": "GOJO Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PURELL Antimicrobial Foaming Hand", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".5 mg/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231211", "listing_expiration_date": "20261231"}