Package 53125-817-29

Brand: north woods derma foam e-2

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 53125-817-29
Digits Only 5312581729
Product NDC 53125-817
Description

1000 mL in 1 BAG (53125-817-29)

Marketing

Marketing Status
Marketed Since 2016-09-15
Brand north woods derma foam e-2
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2736622c-4ecb-472d-e063-6394a90aa9db", "openfda": {"upc": ["0814410022411"], "unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["ab982dec-639a-277a-e053-2a95a90ac8b4"], "manufacturer_name": ["Superior Chemical Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (53125-817-29)", "package_ndc": "53125-817-29", "marketing_start_date": "20160915"}], "brand_name": "North Woods Derma Foam E-2", "product_id": "53125-817_2736622c-4ecb-472d-e063-6394a90aa9db", "dosage_form": "SOAP", "product_ndc": "53125-817", "generic_name": "Benzalkonium Chloride", "labeler_name": "Superior Chemical Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "North Woods Derma Foam E-2", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}