Package 0126-0022-92

Brand: prevident 5000 enamel protect

Generic: sodium fluoride and potassium nitrate
NDC Package

Package Facts

Identity

Package NDC 0126-0022-92
Digits Only 0126002292
Product NDC 0126-0022
Product ID 0126-0022_6b3ab11f-e5c3-460b-8519-1214876dd629
Description

100 mL in 1 BOTTLE (0126-0022-92)

Marketing

Marketing Status
Marketed Since 2011-03-30
Brand prevident 5000 enamel protect
Generic sodium fluoride and potassium nitrate
Sample Package No

Linked Drug Pages (1)

PreviDent 5000 Enamel Protect ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "6b3ab11f-e5c3-460b-8519-1214876dd629", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "spl_set_id": ["bbc66b1b-e05c-4e14-bef3-b8bae419fc89"], "manufacturer_name": ["Colgate Oral Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (0126-0022-92)", "package_ndc": "0126-0022-92", "marketing_start_date": "20110330"}], "brand_name": "PreviDent 5000 Enamel Protect", "product_id": "0126-0022_6b3ab11f-e5c3-460b-8519-1214876dd629", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "0126-0022", "generic_name": "SODIUM FLUORIDE and POTASSIUM NITRATE", "labeler_name": "Colgate Oral Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PreviDent 5000 Enamel Protect", "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": "20110330", "listing_expiration_date": "20261231"}