Package 83986-721-20

Brand: hand sanitizer

Generic: ethyl alcohol
NDC Package

Package Facts

Identity

Package NDC 83986-721-20
Digits Only 8398672120
Product NDC 83986-721
Product ID 83986-721_385144ca-d75a-ffad-e063-6394a90abf5a
Description

59 mL in 1 BOTTLE, SPRAY (83986-721-20)

Marketing

Marketing Status
Marketed Since 2024-04-26
Brand hand sanitizer
Generic ethyl alcohol
Sample Package No

Linked Drug Pages (1)

Hand Sanitizer ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "385144ca-d75a-ffad-e063-6394a90abf5a", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1020364"], "spl_set_id": ["fbfa510c-2cc8-4ac8-95fc-5ac0a2e570ad"], "manufacturer_name": ["UpLift Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, SPRAY (83986-721-20)", "package_ndc": "83986-721-20", "marketing_start_date": "20240426"}], "brand_name": "Hand Sanitizer", "product_id": "83986-721_385144ca-d75a-ffad-e063-6394a90abf5a", "dosage_form": "SPRAY", "product_ndc": "83986-721", "generic_name": "Ethyl Alcohol", "labeler_name": "UpLift Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240426", "listing_expiration_date": "20261231"}