Package 80684-005-01

Brand: ocean breeze scented antibacterial hand sanitizer

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 80684-005-01
Digits Only 8068400501
Product NDC 80684-005
Product ID 80684-005_08a026b8-bede-ca5b-e063-6294a90a0b4e
Description

29 mL in 1 BOTTLE (80684-005-01)

Marketing

Marketing Status
Marketed Since 2020-11-07
Brand ocean breeze scented antibacterial hand sanitizer
Generic alcohol
Sample Package No

Linked Drug Pages (1)

Ocean Breeze Scented Antibacterial Hand Sanitizer ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "08a026b8-bede-ca5b-e063-6294a90a0b4e", "openfda": {"upc": ["0049696504430"], "unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["b3391b8e-877f-e74a-e053-2995a90afd62"], "manufacturer_name": ["Fourstar Group USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE (80684-005-01)", "package_ndc": "80684-005-01", "marketing_start_date": "20201107"}], "brand_name": "Ocean Breeze Scented Antibacterial Hand Sanitizer", "product_id": "80684-005_08a026b8-bede-ca5b-e063-6294a90a0b4e", "dosage_form": "GEL", "product_ndc": "80684-005", "generic_name": "ALCOHOL", "labeler_name": "Fourstar Group USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ocean Breeze Scented Antibacterial Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201107", "listing_expiration_date": "20261231"}