dentisse

Generic: sodium fluoride

Labeler: dentisse, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dentisse
Generic Name sodium fluoride
Labeler dentisse, inc.
Dosage Form PASTE, DENTIFRICE
Routes
DENTAL ORAL
Active Ingredients

sodium fluoride 1.1 mg/g

Manufacturer
Dentisse, Inc.

Identifiers & Regulatory

Product NDC 70683-0703
Product ID 70683-0703_42c83cbe-24d7-6ccb-e063-6294a90ab55b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M021
Listing Expiration 2026-12-31
Marketing Start 2014-02-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 706830703
Hyphenated Format 70683-0703

Supplemental Identifiers

RxCUI
891775
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 dentisse (source: ndc)
Generic Name sodium fluoride (source: ndc)
Application Number M021 (source: ndc)
Routes
DENTAL ORAL
source: ndc

Resolved Composition

Strengths
  • 1.1 mg/g
source: ndc
Packaging
  • 91 g in 1 TUBE (70683-0703-2)
source: ndc

Packages (1)

Ingredients (1)

sodium fluoride (1.1 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL", "ORAL"], "spl_id": "42c83cbe-24d7-6ccb-e063-6294a90ab55b", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["891775"], "spl_set_id": ["326b290a-9bd2-468e-e054-00144ff8d46c"], "manufacturer_name": ["Dentisse, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "91 g in 1 TUBE (70683-0703-2)", "package_ndc": "70683-0703-2", "marketing_start_date": "20140213"}], "brand_name": "Dentisse", "product_id": "70683-0703_42c83cbe-24d7-6ccb-e063-6294a90ab55b", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "70683-0703", "generic_name": "Sodium Fluoride", "labeler_name": "Dentisse, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dentisse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "1.1 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140213", "listing_expiration_date": "20261231"}