Package 21749-028-01

Brand: purell advanced hand sanitizer be vibrant

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 21749-028-01
Digits Only 2174902801
Product NDC 21749-028
Product ID 21749-028_48366d7a-55a5-901e-e063-6294a90a677d
Description

30 mL in 1 PACKAGE (21749-028-01)

Marketing

Marketing Status
Marketed Since 2016-12-22
Brand purell advanced hand sanitizer be vibrant
Generic alcohol
Sample Package No

Linked Drug Pages (1)

PURELL Advanced Hand Sanitizer be Vibrant ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "48366d7a-55a5-901e-e063-6294a90a677d", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["3a991a7f-1289-4aeb-82f9-8cebd6a389b5"], "manufacturer_name": ["GOJO Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 PACKAGE (21749-028-01)", "package_ndc": "21749-028-01", "marketing_start_date": "20161222"}], "brand_name": "PURELL Advanced Hand Sanitizer be Vibrant", "product_id": "21749-028_48366d7a-55a5-901e-e063-6294a90a677d", "dosage_form": "GEL", "product_ndc": "21749-028", "generic_name": "alcohol", "labeler_name": "GOJO Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PURELL Advanced Hand Sanitizer be Vibrant", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161222", "listing_expiration_date": "20271231"}