Package 51326-900-08
Brand: sanix alcohol hand rub
Generic: alcoholPackage Facts
Identity
Package NDC
51326-900-08
Digits Only
5132690008
Product NDC
51326-900
Description
240 mL in 1 BOTTLE (51326-900-08)
Marketing
Marketing Status
Brand
sanix alcohol hand rub
Generic
alcohol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2af17da6-253d-4958-92ce-2dc70987b669", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["a4fbb714-4f20-400a-ab98-f1c8807ce6fc"], "manufacturer_name": ["Topiderm, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (51326-900-08)", "package_ndc": "51326-900-08", "marketing_start_date": "20200317"}], "brand_name": "Sanix Alcohol Hand Rub", "product_id": "51326-900_2af17da6-253d-4958-92ce-2dc70987b669", "dosage_form": "LIQUID", "product_ndc": "51326-900", "generic_name": "Alcohol", "labeler_name": "Topiderm, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sanix Alcohol Hand Rub", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200317", "listing_expiration_date": "20261231"}