Package 71020-030-64

Brand: antibacterial aqua clear 2x ultra

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 71020-030-64
Digits Only 7102003064
Product NDC 71020-030
Description

1900 mL in 1 BOTTLE, PLASTIC (71020-030-64)

Marketing

Marketing Status
Marketed Since 2016-10-08
Brand antibacterial aqua clear 2x ultra
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2b21995e-29b7-a54c-e063-6394a90aa3e7", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["d5d15729-1dc1-2b44-e053-2a95a90a26c5"], "manufacturer_name": ["Sante Manufacturing Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "600 mL in 1 BOTTLE, PLASTIC (71020-030-30)", "package_ndc": "71020-030-30", "marketing_start_date": "20161008"}, {"sample": false, "description": "1900 mL in 1 BOTTLE, PLASTIC (71020-030-64)", "package_ndc": "71020-030-64", "marketing_start_date": "20161008"}], "brand_name": "Antibacterial Aqua Clear 2X Ultra", "product_id": "71020-030_2b21995e-29b7-a54c-e063-6394a90aa3e7", "dosage_form": "LIQUID", "product_ndc": "71020-030", "generic_name": "Benzalkonium Chloride", "labeler_name": "Sante Manufacturing Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antibacterial Aqua Clear", "brand_name_suffix": "2X Ultra", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161008", "listing_expiration_date": "20261231"}