Package 63998-764-02

Brand: alcohol-free hand sanitizing foam

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 63998-764-02
Digits Only 6399876402
Product NDC 63998-764
Product ID 63998-764_27c4d6fe-7567-073f-e063-6394a90afe9f
Description

750 mL in 1 BOTTLE (63998-764-02)

Marketing

Marketing Status
Marketed Since 2019-01-01
Brand alcohol-free hand sanitizing foam
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Alcohol-Free Hand Sanitizing Foam ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "27c4d6fe-7567-073f-e063-6394a90afe9f", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1038799"], "spl_set_id": ["4f5ddead-1868-45c2-9657-762c9ca3a0e2"], "manufacturer_name": ["United Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE (63998-764-01)", "package_ndc": "63998-764-01", "marketing_start_date": "20190101"}, {"sample": false, "description": "750 mL in 1 BOTTLE (63998-764-02)", "package_ndc": "63998-764-02", "marketing_start_date": "20190101"}], "brand_name": "Alcohol-Free Hand Sanitizing Foam", "product_id": "63998-764_27c4d6fe-7567-073f-e063-6394a90afe9f", "dosage_form": "SOLUTION", "product_ndc": "63998-764", "generic_name": "BENZALKONIUM CHLORIDE", "labeler_name": "United Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol-Free Hand Sanitizing Foam", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}