medichoice fluoride
Generic: sodium monofluorophosphate
Labeler: o&m halyard, inc.Drug Facts
Product Profile
Brand Name
medichoice fluoride
Generic Name
sodium monofluorophosphate
Labeler
o&m halyard, inc.
Dosage Form
PASTE, DENTIFRICE
Routes
Active Ingredients
sodium monofluorophosphate 7.6 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
39892-0602
Product ID
39892-0602_40b535d8-2de7-7246-e063-6294a90a7c9b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2013-03-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
398920602
Hyphenated Format
39892-0602
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
medichoice fluoride (source: ndc)
Generic Name
sodium monofluorophosphate (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 7.6 mg/g
Packaging
- 17 g in 1 TUBE (39892-0602-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "40b535d8-2de7-7246-e063-6294a90a7c9b", "openfda": {"unii": ["C810JCZ56Q"], "rxcui": ["545626"], "spl_set_id": ["a87956fa-8975-4a44-9e9a-4b2191e401fe"], "manufacturer_name": ["O&M HALYARD, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "17 g in 1 TUBE (39892-0602-1)", "package_ndc": "39892-0602-1", "marketing_start_date": "20130301"}], "brand_name": "MediChoice Fluoride", "product_id": "39892-0602_40b535d8-2de7-7246-e063-6294a90a7c9b", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "39892-0602", "generic_name": "SODIUM MONOFLUOROPHOSPHATE", "labeler_name": "O&M HALYARD, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MediChoice Fluoride", "active_ingredients": [{"name": "SODIUM MONOFLUOROPHOSPHATE", "strength": "7.6 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}