Package 16571-823-10

Brand: denta 5000 plus sensitive

Generic: sodium fluoride and potassium nitrate
NDC Package

Package Facts

Identity

Package NDC 16571-823-10
Digits Only 1657182310
Product NDC 16571-823
Product ID 16571-823_3d38b4ec-9283-448f-8fc5-d51cca9de7a6
Description

100 mL in 1 TUBE (16571-823-10)

Marketing

Marketing Status
Marketed Since 2024-02-14
Brand denta 5000 plus sensitive
Generic sodium fluoride and potassium nitrate
Sample Package No

Linked Drug Pages (1)

Denta 5000 Plus Sensitive ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "3d38b4ec-9283-448f-8fc5-d51cca9de7a6", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "spl_set_id": ["585fb1f5-8c08-43bd-8be4-64adc065d9a2"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 TUBE (16571-823-10)", "package_ndc": "16571-823-10", "marketing_start_date": "20240214"}], "brand_name": "Denta 5000 Plus Sensitive", "product_id": "16571-823_3d38b4ec-9283-448f-8fc5-d51cca9de7a6", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "16571-823", "generic_name": "Sodium fluoride and Potassium nitrate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Denta 5000 Plus 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": "20240214", "listing_expiration_date": "20261231"}