Package 80586-801-04

Brand: beverly gel hand sanitizer

Generic: ethyl alcohol
NDC Package

Package Facts

Identity

Package NDC 80586-801-04
Digits Only 8058680104
Product NDC 80586-801
Product ID 80586-801_40a7834b-0c0a-e8ca-e063-6294a90a5afd
Description

3785 mL in 1 BOTTLE, PLASTIC (80586-801-04)

Marketing

Marketing Status
Marketed Since 2024-01-10
Brand beverly gel hand sanitizer
Generic ethyl alcohol
Sample Package No

Linked Drug Pages (1)

Beverly Gel Hand Sanitizer ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "40a7834b-0c0a-e8ca-e063-6294a90a5afd", "openfda": {"upc": ["0850041389783"], "unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["0e999251-cb51-ceec-e063-6294a90a35ad"], "manufacturer_name": ["Cleanslate Group LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3785 mL in 1 BOTTLE, PLASTIC (80586-801-04)", "package_ndc": "80586-801-04", "marketing_start_date": "20240110"}], "brand_name": "Beverly Gel Hand Sanitizer", "product_id": "80586-801_40a7834b-0c0a-e8ca-e063-6294a90a5afd", "dosage_form": "GEL", "product_ndc": "80586-801", "generic_name": "ethyl alcohol", "labeler_name": "Cleanslate Group LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Beverly Gel Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240110", "listing_expiration_date": "20261231"}