Package 83986-015-32

Brand: antibacterial hand wash

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 83986-015-32
Digits Only 8398601532
Product NDC 83986-015
Description

355 mL in 1 BOTTLE, PUMP (83986-015-32)

Marketing

Marketing Status
Marketed Since 2022-10-14
Brand antibacterial hand wash
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "39e45956-951c-b4cd-e063-6394a90a3b1a", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["2e9a5253-f68d-4db5-a479-2663fc7789af"], "manufacturer_name": ["UpLift Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE, PUMP (83986-015-32)", "package_ndc": "83986-015-32", "marketing_start_date": "20221014"}], "brand_name": "Antibacterial Hand Wash", "product_id": "83986-015_39e45956-951c-b4cd-e063-6394a90a3b1a", "dosage_form": "SOAP", "product_ndc": "83986-015", "generic_name": "Benzalkonium chloride", "labeler_name": "UpLift Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antibacterial Hand Wash", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221014", "listing_expiration_date": "20261231"}