denta 5000 plus sensitive
Generic: sodium fluoride and potassium nitrate
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
denta 5000 plus sensitive
Generic Name
sodium fluoride and potassium nitrate
Labeler
rising pharma holdings, inc.
Dosage Form
GEL, DENTIFRICE
Routes
Active Ingredients
potassium nitrate 57.5 mg/mL, sodium fluoride 5.8 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
16571-823
Product ID
16571-823_3d38b4ec-9283-448f-8fc5-d51cca9de7a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2024-02-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16571823
Hyphenated Format
16571-823
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
denta 5000 plus sensitive (source: ndc)
Generic Name
sodium fluoride and potassium nitrate (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 57.5 mg/mL
- 5.8 mg/mL
Packaging
- 100 mL in 1 TUBE (16571-823-10)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
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"}