Package 42961-224-71

Brand: foaming hand

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 42961-224-71
Digits Only 4296122471
Product NDC 42961-224
Product ID 42961-224_49dac8e8-231b-6f18-e063-6394a90aecd1
Description

800 mL in 1 BOTTLE, PUMP (42961-224-71)

Marketing

Marketing Status
Marketed Since 2020-07-20
Brand foaming hand
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Foaming Hand ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "49dac8e8-231b-6f18-e063-6394a90aecd1", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["17fb34e7-c9e6-41aa-991f-bb54c84ed79c"], "manufacturer_name": ["Cintas Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "800 mL in 1 BOTTLE, PUMP (42961-224-71)", "package_ndc": "42961-224-71", "marketing_start_date": "20200720"}], "brand_name": "Foaming Hand", "product_id": "42961-224_49dac8e8-231b-6f18-e063-6394a90aecd1", "dosage_form": "LOTION", "product_ndc": "42961-224", "generic_name": "Benzalkonium Chloride", "labeler_name": "Cintas Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foaming Hand", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200720", "listing_expiration_date": "20271231"}