universal sensitive anti-cavity fluoride
Generic: potassium nitrate and sodium fluoride
Labeler: universal distribution center llcDrug Facts
Product Profile
Brand Name
universal sensitive anti-cavity fluoride
Generic Name
potassium nitrate and sodium fluoride
Labeler
universal distribution center llc
Dosage Form
PASTE
Routes
Active Ingredients
potassium nitrate 5 g/100g, sodium fluoride .15 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
52000-109
Product ID
52000-109_1199f2f8-98e4-4b76-9be9-3b921495a3c3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2026-12-31
Marketing Start
2020-05-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52000109
Hyphenated Format
52000-109
Supplemental Identifiers
RxCUI
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
universal sensitive anti-cavity fluoride (source: ndc)
Generic Name
potassium nitrate and sodium fluoride (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 g/100g
- .15 g/100g
Packaging
- 122 g in 1 TUBE (52000-109-01)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
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"}