fluoridex

Generic: sodium fluoride

Labeler: den-mat holdings, llc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name fluoridex
Generic Name sodium fluoride
Labeler den-mat holdings, llc.
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL
Active Ingredients

sodium fluoride 5 mg/g

Manufacturer
DEN-MAT HOLDINGS, LLC.

Identifiers & Regulatory

Product NDC 59883-020
Product ID 59883-020_82f8eacb-a214-3080-e053-2a91aa0a6a07
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2017-01-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59883020
Hyphenated Format 59883-020

Supplemental Identifiers

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 fluoridex (source: ndc)
Generic Name sodium fluoride (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 BOX (59883-020-04) / 112 g in 1 TUBE
source: ndc

Packages (1)

59883-020-04 1 TUBE in 1 BOX (59883-020-04) / 112 g in 1 TUBE

Ingredients (1)

sodium fluoride (5 mg/g)

Linked Drug Pages (1)

FLUORIDEX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "82f8eacb-a214-3080-e053-2a91aa0a6a07", "openfda": {"unii": ["8ZYQ1474W7"], "spl_set_id": ["6014c330-3698-027c-e053-2a91aa0a64e5"], "manufacturer_name": ["DEN-MAT HOLDINGS, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (59883-020-04)  / 112 g in 1 TUBE", "package_ndc": "59883-020-04", "marketing_start_date": "20170103"}], "brand_name": "FLUORIDEX", "product_id": "59883-020_82f8eacb-a214-3080-e053-2a91aa0a6a07", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "59883-020", "generic_name": "Sodium Fluoride", "labeler_name": "DEN-MAT HOLDINGS, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUORIDEX", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "5 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20170103", "listing_expiration_date": "20261231"}