ortho super mint fluoride mouthwash
Generic: anticavity mouthwash
Labeler: supermouth, llc.Drug Facts
Product Profile
Brand Name
ortho super mint fluoride mouthwash
Generic Name
anticavity mouthwash
Labeler
supermouth, llc.
Dosage Form
LIQUID
Routes
Active Ingredients
sodium fluoride .002 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
83729-110
Product ID
83729-110_07e8e2fd-6bf0-4cbc-8fcf-f3d4ce5329ca
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2023-02-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83729110
Hyphenated Format
83729-110
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
ortho super mint fluoride mouthwash (source: ndc)
Generic Name
anticavity mouthwash (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .002 mg/10mL
Packaging
- 473 mL in 1 BOTTLE (83729-110-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "07e8e2fd-6bf0-4cbc-8fcf-f3d4ce5329ca", "openfda": {"unii": ["8ZYQ1474W7"], "spl_set_id": ["e50c3723-4af3-4e5e-a194-5a8a5ebe5d01"], "manufacturer_name": ["SuperMouth, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (83729-110-16)", "package_ndc": "83729-110-16", "marketing_start_date": "20230221"}], "brand_name": "Ortho Super Mint Fluoride Mouthwash", "product_id": "83729-110_07e8e2fd-6bf0-4cbc-8fcf-f3d4ce5329ca", "dosage_form": "LIQUID", "product_ndc": "83729-110", "generic_name": "Anticavity Mouthwash", "labeler_name": "SuperMouth, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ortho Super Mint Fluoride Mouthwash", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".002 mg/10mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230221", "listing_expiration_date": "20261231"}