sodium fluoride 1.1% gel

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 1.1% gel
Generic Name sodium fluoride
Labeler westminster pharmaceuticals, llc
Dosage Form GEL
Routes
DENTAL
Active Ingredients

sodium fluoride 5 mg/g

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-310
Product ID 69367-310_4251b577-cd67-4556-a1cc-207aea831860
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2021-03-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367310
Hyphenated Format 69367-310

Supplemental Identifiers

RxCUI
1486566
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 1.1% gel (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 CARTON (69367-310-56) / 56 g in 1 TUBE
source: ndc

Packages (1)

69367-310-56 1 TUBE in 1 CARTON (69367-310-56) / 56 g in 1 TUBE

Ingredients (1)

sodium fluoride (5 mg/g)

Linked Drug Pages (1)

Sodium Fluoride 1.1% Gel ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "4251b577-cd67-4556-a1cc-207aea831860", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1486566"], "spl_set_id": ["1822c957-0bd6-4e86-a030-80e6e428063a"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69367-310-56)  / 56 g in 1 TUBE", "package_ndc": "69367-310-56", "marketing_start_date": "20210309"}], "brand_name": "Sodium Fluoride 1.1% Gel", "product_id": "69367-310_4251b577-cd67-4556-a1cc-207aea831860", "dosage_form": "GEL", "product_ndc": "69367-310", "generic_name": "Sodium Fluoride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride 1.1% Gel", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "5 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210309", "listing_expiration_date": "20261231"}