Package 79631-000-00
Brand: hand sanitizer
Generic: alcoholPackage Facts
Identity
Package NDC
79631-000-00
Digits Only
7963100000
Product NDC
79631-000
Description
35 mL in 1 BOTTLE (79631-000-00)
Marketing
Marketing Status
Brand
hand sanitizer
Generic
alcohol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0899cafe-9050-8a8e-e063-6394a90a1f0e", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1305100"], "spl_set_id": ["5033fcad-fb65-45b8-a4ec-c7b2c9d11793"], "manufacturer_name": ["Andaz Group LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "35 mL in 1 BOTTLE (79631-000-00)", "package_ndc": "79631-000-00", "marketing_start_date": "20200718"}], "brand_name": "HAND SANITIZER", "product_id": "79631-000_0899cafe-9050-8a8e-e063-6394a90a1f0e", "dosage_form": "GEL", "product_ndc": "79631-000", "generic_name": "ALCOHOL", "labeler_name": "Andaz Group LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HAND SANITIZER", "active_ingredients": [{"name": "ALCOHOL", "strength": ".75 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200718", "listing_expiration_date": "20261231"}