Package 52000-801-01

Brand: isopropyl rubbing alcohol

Generic: isopropyl alcohol
NDC Package

Package Facts

Identity

Package NDC 52000-801-01
Digits Only 5200080101
Product NDC 52000-801
Description

355 mL in 1 BOTTLE, PLASTIC (52000-801-01)

Marketing

Marketing Status
Marketed Since 2012-06-29
Brand isopropyl rubbing alcohol
Generic isopropyl alcohol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2f982a20-e80a-a5a5-e063-6394a90a95f4", "openfda": {"upc": ["0676979556048"], "unii": ["ND2M416302"], "rxcui": ["616456"], "spl_set_id": ["2f982aef-4f46-aa85-e063-6394a90a52b1"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (52000-801-01)", "package_ndc": "52000-801-01", "marketing_start_date": "20120629"}, {"sample": false, "description": "946 mL in 1 BOTTLE, PLASTIC (52000-801-02)", "package_ndc": "52000-801-02", "marketing_start_date": "20120629"}], "brand_name": "Isopropyl Rubbing Alcohol", "product_id": "52000-801_2f982a20-e80a-a5a5-e063-6394a90a95f4", "dosage_form": "LIQUID", "product_ndc": "52000-801", "generic_name": "Isopropyl Alcohol", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Isopropyl Rubbing Alcohol", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": "50 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120629", "listing_expiration_date": "20261231"}