sodium fluoride

Generic: sodium fluoride

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

Drug Facts

Product Profile

Brand Name sodium fluoride
Generic Name sodium fluoride
Labeler method pharmaceuticals, llc
Dosage Form SOLUTION/ DROPS
Routes
ORAL
Active Ingredients

sodium fluoride .5 mg/mL

Manufacturer
Method Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 58657-322
Product ID 58657-322_41b6cf2b-2810-7774-e063-6394a90ac1fb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2018-08-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58657322
Hyphenated Format 58657-322

Supplemental Identifiers

RxCUI
315102
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 (source: ndc)
Generic Name sodium fluoride (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE, DROPPER (58657-322-50)
source: ndc

Packages (1)

58657-322-50 50 mL in 1 BOTTLE, DROPPER (58657-322-50)

Ingredients (1)

sodium fluoride (.5 mg/mL)

Linked Drug Pages (1)

Sodium Fluoride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41b6cf2b-2810-7774-e063-6394a90ac1fb", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["315102"], "spl_set_id": ["35dcc144-130d-4ec7-a266-c084008ac70c"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE, DROPPER (58657-322-50)", "package_ndc": "58657-322-50", "marketing_start_date": "20180815"}], "brand_name": "Sodium Fluoride", "product_id": "58657-322_41b6cf2b-2810-7774-e063-6394a90ac1fb", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "58657-322", "generic_name": "Sodium Fluoride", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".5 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20180815", "listing_expiration_date": "20261231"}