pro-den rx

Generic: sodium fluoride

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

Drug Facts

Product Profile

Brand Name pro-den rx
Generic Name sodium fluoride
Labeler den-mat holdings, llc
Dosage Form RINSE
Routes
ORAL
Active Ingredients

sodium fluoride .9 mg/mL

Manufacturer
Den-mat Holdings, Llc

Identifiers & Regulatory

Product NDC 59883-920
Product ID 59883-920_82f8dd55-36df-0de0-e053-2991aa0a6bbf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2008-10-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59883920
Hyphenated Format 59883-920

Supplemental Identifiers

RxCUI
562510 1488074
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 pro-den rx (source: ndc)
Generic Name sodium fluoride (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .9 mg/mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (59883-920-16)
source: ndc

Packages (1)

59883-920-16 473 mL in 1 BOTTLE, PLASTIC (59883-920-16)

Ingredients (1)

sodium fluoride (.9 mg/mL)

Linked Drug Pages (1)

Pro-Den Rx ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "82f8dd55-36df-0de0-e053-2991aa0a6bbf", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["562510", "1488074"], "spl_set_id": ["e39b19f7-2b3e-4c77-9544-623ebad84870"], "manufacturer_name": ["Den-mat Holdings, Llc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (59883-920-16)", "package_ndc": "59883-920-16", "marketing_start_date": "20081021"}], "brand_name": "Pro-Den Rx", "product_id": "59883-920_82f8dd55-36df-0de0-e053-2991aa0a6bbf", "dosage_form": "RINSE", "product_ndc": "59883-920", "generic_name": "Sodium Fluoride", "labeler_name": "Den-mat Holdings, Llc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pro-Den Rx", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".9 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20081021", "listing_expiration_date": "20261231"}