dentisse
Generic: sodium fluoride
Labeler: dentisse, inc.Drug Facts
Product Profile
Brand Name
dentisse
Generic Name
sodium fluoride
Labeler
dentisse, inc.
Dosage Form
PASTE, DENTIFRICE
Routes
Active Ingredients
sodium fluoride 1.1 mg/g
Manufacturer
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
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1.1 mg/g
Packaging
- 91 g in 1 TUBE (70683-0703-2)
Packages (1)
Ingredients (1)
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"}