Package 47593-692-70

Brand: exp foaming hand sanitizer

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 47593-692-70
Digits Only 4759369270
Product NDC 47593-692
Product ID 47593-692_3edaece0-b4c4-46fe-bbbe-fca72128eafd
Description

1200 mL in 1 BOTTLE, PLASTIC (47593-692-70)

Marketing

Marketing Status
Marketed Since 2025-12-30
Brand exp foaming hand sanitizer
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

EXP Foaming Hand Sanitizer ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3edaece0-b4c4-46fe-bbbe-fca72128eafd", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["468acf2d-97ff-4cac-91b1-067a1ea382f3"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1200 mL in 1 BOTTLE, PLASTIC (47593-692-70)", "package_ndc": "47593-692-70", "marketing_start_date": "20251230"}], "brand_name": "EXP Foaming Hand Sanitizer", "product_id": "47593-692_3edaece0-b4c4-46fe-bbbe-fca72128eafd", "dosage_form": "SOLUTION", "product_ndc": "47593-692", "generic_name": "Benzalkonium chloride", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXP Foaming Hand Sanitizer", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".1 mg/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251230", "listing_expiration_date": "20261231"}