Package 80684-001-01

Brand: p b pure antibacterial hand sanitizer ocean breeze scented

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 80684-001-01
Digits Only 8068400101
Product NDC 80684-001
Description

29 mL in 1 BOTTLE (80684-001-01)

Marketing

Marketing Status
Marketed Since 2020-09-24
Brand p b pure antibacterial hand sanitizer ocean breeze scented
Generic alcohol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "089fffdd-2eed-6928-e063-6294a90af1c6", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["902574"], "spl_set_id": ["b17d3da6-a0f8-55d2-e053-2995a90a6ab9"], "manufacturer_name": ["FOURSTAR GROUP USA, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE (80684-001-01)", "package_ndc": "80684-001-01", "marketing_start_date": "20200924"}], "brand_name": "P b pure Antibacterial Hand Sanitizer Ocean Breeze Scented", "product_id": "80684-001_089fffdd-2eed-6928-e063-6294a90af1c6", "dosage_form": "GEL", "product_ndc": "80684-001", "generic_name": "ALCOHOL", "labeler_name": "FOURSTAR GROUP USA, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "P b pure Antibacterial Hand Sanitizer Ocean Breeze Scented", "active_ingredients": [{"name": "ALCOHOL", "strength": ".65 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}