Package 0126-0070-61

Brand: prevident 5000 sensitive

Generic: sodium fluoride and potassium nitrate
NDC Package

Package Facts

Identity

Package NDC 0126-0070-61
Digits Only 0126007061
Product NDC 0126-0070
Product ID 0126-0070_9d1b6e76-002b-49e4-b483-be15723a03d6
Description

100 mL in 1 BOTTLE (0126-0070-61)

Marketing

Marketing Status
Marketed Since 2009-07-06
Brand prevident 5000 sensitive
Generic sodium fluoride and potassium nitrate
Sample Package No

Linked Drug Pages (1)

PreviDent 5000 Sensitive ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "9d1b6e76-002b-49e4-b483-be15723a03d6", "openfda": {"upc": ["0301260070612"], "unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["637365", "999717"], "spl_set_id": ["b028cfff-4946-49e8-b8bb-197ab99d0d35"], "manufacturer_name": ["Colgate Oral Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (0126-0070-61)", "package_ndc": "0126-0070-61", "marketing_start_date": "20090706"}], "brand_name": "PreviDent 5000 Sensitive", "product_id": "0126-0070_9d1b6e76-002b-49e4-b483-be15723a03d6", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "0126-0070", "generic_name": "Sodium fluoride and Potassium nitrate", "labeler_name": "Colgate Oral Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PreviDent", "brand_name_suffix": "5000 Sensitive", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "57.5 mg/mL"}, {"name": "SODIUM FLUORIDE", "strength": "5.8 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20090706", "listing_expiration_date": "20261231"}