sodium fluoride 5000 ppm

Generic: sodium fluoride

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name sodium fluoride 5000 ppm
Generic Name sodium fluoride
Labeler westminster pharmaceuticals, llc
Dosage Form PASTE
Routes
DENTAL
Active Ingredients

sodium fluoride 6 mg/mL

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-312
Product ID 69367-312_f227132c-6257-4245-b8e0-7de78c15c201
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2021-06-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367312
Hyphenated Format 69367-312

Supplemental Identifiers

RxCUI
392038
UNII
8ZYQ1474W7

Packaging Origin

Original Packager
true

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 sodium fluoride 5000 ppm (source: ndc)
Generic Name sodium fluoride (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 6 mg/mL
source: ndc
Packaging
  • 100 mL in 1 TUBE (69367-312-01)
source: ndc

Packages (1)

69367-312-01 100 mL in 1 TUBE (69367-312-01)

Ingredients (1)

sodium fluoride (6 mg/mL)

Linked Drug Pages (1)

Sodium Fluoride 5000 PPM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "f227132c-6257-4245-b8e0-7de78c15c201", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["392038"], "spl_set_id": ["56efb346-c715-463d-9260-f7fcfbd2b70f"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 TUBE (69367-312-01)", "package_ndc": "69367-312-01", "marketing_start_date": "20210616"}], "brand_name": "Sodium Fluoride 5000 PPM", "product_id": "69367-312_f227132c-6257-4245-b8e0-7de78c15c201", "dosage_form": "PASTE", "product_ndc": "69367-312", "generic_name": "Sodium Fluoride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride 5000 PPM", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "6 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210616", "listing_expiration_date": "20261231"}