Package 51142-444-01

Brand: alcohol prep pad

Generic: alcohol prep pad
NDC Package

Package Facts

Identity

Package NDC 51142-444-01
Digits Only 5114244401
Product NDC 51142-444
Description

.4 mL in 1 POUCH (51142-444-01)

Marketing

Marketing Status
Marketed Since 2018-09-24
Brand alcohol prep pad
Generic alcohol prep pad
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "25da293c-7ff5-8fe3-e063-6394a90a9af1", "openfda": {"unii": ["ND2M416302"], "spl_set_id": ["7481bfb9-2baf-b1ec-e053-2991aa0ad2de"], "manufacturer_name": ["ASO LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".4 mL in 1 POUCH (51142-444-01)", "package_ndc": "51142-444-01", "marketing_start_date": "20180924"}], "brand_name": "Alcohol Prep Pad", "product_id": "51142-444_25da293c-7ff5-8fe3-e063-6394a90a9af1", "dosage_form": "LIQUID", "product_ndc": "51142-444", "generic_name": "Alcohol Prep Pad", "labeler_name": "ASO LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol Prep Pad", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180924", "listing_expiration_date": "20261231"}