emmi-dent whitening
Generic: sodium fluoride
Labeler: emag agDrug Facts
Product Profile
Brand Name
emmi-dent whitening
Generic Name
sodium fluoride
Labeler
emag ag
Dosage Form
PASTE, DENTIFRICE
Routes
Active Ingredients
sodium fluoride 320 mg/75mL
Manufacturer
Identifiers & Regulatory
Product NDC
63956-003
Product ID
63956-003_407a5a0e-64d8-43cb-8d24-644261870049
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2019-07-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63956003
Hyphenated Format
63956-003
Supplemental Identifiers
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
emmi-dent whitening (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 320 mg/75mL
Packaging
- 1 TUBE in 1 CARTON (63956-003-03) / 75 mL in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "407a5a0e-64d8-43cb-8d24-644261870049", "openfda": {"unii": ["8ZYQ1474W7"], "spl_set_id": ["dbc0cfe0-24ef-4ee2-b975-4044624a592f"], "manufacturer_name": ["EMAG AG"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (63956-003-03) / 75 mL in 1 TUBE", "package_ndc": "63956-003-03", "marketing_start_date": "20190730"}], "brand_name": "Emmi-dent Whitening", "product_id": "63956-003_407a5a0e-64d8-43cb-8d24-644261870049", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "63956-003", "generic_name": "Sodium Fluoride", "labeler_name": "EMAG AG", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Emmi-dent Whitening", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "320 mg/75mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190730", "listing_expiration_date": "20261231"}