Package 52000-109-01

Brand: universal sensitive anti-cavity fluoride

Generic: potassium nitrate and sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 52000-109-01
Digits Only 5200010901
Product NDC 52000-109
Product ID 52000-109_1199f2f8-98e4-4b76-9be9-3b921495a3c3
Description

122 g in 1 TUBE (52000-109-01)

Marketing

Marketing Status
Marketed Since 2020-05-20
Brand universal sensitive anti-cavity fluoride
Generic potassium nitrate and sodium fluoride
Sample Package No

Linked Drug Pages (1)

UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "1199f2f8-98e4-4b76-9be9-3b921495a3c3", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1038841"], "spl_set_id": ["fcf59439-7e06-4129-a89f-cdeecdf8d488"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "122 g in 1 TUBE (52000-109-01)", "package_ndc": "52000-109-01", "marketing_start_date": "20200520"}], "brand_name": "UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE", "product_id": "52000-109_1199f2f8-98e4-4b76-9be9-3b921495a3c3", "dosage_form": "PASTE", "product_ndc": "52000-109", "generic_name": "potassium nitrate and sodium fluoride", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "5 g/100g"}, {"name": "SODIUM FLUORIDE", "strength": ".15 g/100g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200520", "listing_expiration_date": "20261231"}