super strawberry fluoride mouthwash
Generic: anticavity mouthwash
Labeler: supermouth, llc.Drug Facts
Product Profile
Brand Name
super strawberry 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
83729-105
Product ID
83729-105_a7b235cc-1007-4988-9a57-858c9cc16afd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2023-03-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83729105
Hyphenated Format
83729-105
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
super strawberry 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 (83729-105-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "a7b235cc-1007-4988-9a57-858c9cc16afd", "openfda": {"unii": ["8ZYQ1474W7"], "spl_set_id": ["a56f51e1-38b5-4487-82dd-af39f8cb9b16"], "manufacturer_name": ["SuperMouth, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (83729-105-16)", "package_ndc": "83729-105-16", "marketing_start_date": "20230321"}], "brand_name": "Super Strawberry Fluoride Mouthwash", "product_id": "83729-105_a7b235cc-1007-4988-9a57-858c9cc16afd", "dosage_form": "LIQUID", "product_ndc": "83729-105", "generic_name": "Anticavity Mouthwash", "labeler_name": "SuperMouth, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Super Strawberry Fluoride Mouthwash", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".002 mg/10mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230321", "listing_expiration_date": "20261231"}