Package 83986-439-32

Brand: advanced hand sanitizer

Generic: ethyl alcohol
NDC Package

Package Facts

Identity

Package NDC 83986-439-32
Digits Only 8398643932
Product NDC 83986-439
Description

355 mL in 1 BOTTLE, PLASTIC (83986-439-32)

Marketing

Marketing Status
Marketed Since 2024-02-23
Brand advanced hand sanitizer
Generic ethyl alcohol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4cc421e7-7f44-05e2-e063-6394a90a51c1", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["f6608379-051f-4151-bcf7-ecd87070f439"], "manufacturer_name": ["UpLift Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, DISPENSING (83986-439-16)", "package_ndc": "83986-439-16", "marketing_start_date": "20240223"}, {"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (83986-439-32)", "package_ndc": "83986-439-32", "marketing_start_date": "20240223"}, {"sample": false, "description": "236 mL in 1 BOTTLE, PUMP (83986-439-34)", "package_ndc": "83986-439-34", "marketing_start_date": "20240223"}, {"sample": false, "description": "709 mL in 1 BOTTLE, PLASTIC (83986-439-50)", "package_ndc": "83986-439-50", "marketing_start_date": "20240223"}, {"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (83986-439-86)", "package_ndc": "83986-439-86", "marketing_start_date": "20240223"}], "brand_name": "Advanced Hand Sanitizer", "product_id": "83986-439_4cc421e7-7f44-05e2-e063-6394a90a51c1", "dosage_form": "GEL", "product_ndc": "83986-439", "generic_name": "Ethyl Alcohol", "labeler_name": "UpLift Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240223", "listing_expiration_date": "20271231"}