Fluoride

Generic: Sodium Fluoride

Labeler: PureTek Corporation
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive

Drug Facts

Product Profile

Brand Name Fluoride
Generic Name Sodium Fluoride
Labeler PureTek Corporation
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

SODIUM FLUORIDE .5 mg/1

Identifiers & Regulatory

Product NDC 59088-105
Product ID 59088-105_2b4c6983-d7f6-5873-e063-6294a90a0c8f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Marketing Start 2011-06-01
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59088105
Hyphenated Format 59088-105

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 Fluoride (source: ndc)
Generic Name Sodium Fluoride (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-105-73)
source: ndc

Packages (1)

59088-105-73 120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-105-73)

Ingredients (1)

SODIUM FLUORIDE (.5 mg/1)

Linked Drug Pages (1)

Fluoride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b4c6983-d7f6-5873-e063-6294a90a0c8f", "openfda": {"upc": ["0731477421776"], "unii": ["8ZYQ1474W7"], "rxcui": ["313036"], "spl_set_id": ["75d61626-753b-435a-b6d6-503da08e3733"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-105-73)", "package_ndc": "59088-105-73", "marketing_end_date": "20260228", "marketing_start_date": "20110601"}], "brand_name": "Fluoride", "product_id": "59088-105_2b4c6983-d7f6-5873-e063-6294a90a0c8f", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "59088-105", "generic_name": "Sodium Fluoride", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoride", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".5 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_end_date": "20260228", "marketing_start_date": "20110601"}