anticavity rinse
Generic: sodium fluoride
Labeler: meijer, inc.Drug Facts
Product Profile
Brand Name
anticavity rinse
Generic Name
sodium fluoride
Labeler
meijer, inc.
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
79481-0201
Product ID
79481-0201_4b3247ad-5a19-94db-e063-6394a90a006f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2021-07-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
794810201
Hyphenated Format
79481-0201
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
anticavity rinse (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/mL
Packaging
- 532 mL in 1 BOTTLE, PLASTIC (79481-0201-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b3247ad-5a19-94db-e063-6394a90a006f", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["b17f7a5d-272e-446d-803b-46a6d8e5f18f"], "manufacturer_name": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "532 mL in 1 BOTTLE, PLASTIC (79481-0201-1)", "package_ndc": "79481-0201-1", "marketing_start_date": "20210714"}], "brand_name": "Anticavity Rinse", "product_id": "79481-0201_4b3247ad-5a19-94db-e063-6394a90a006f", "dosage_form": "MOUTHWASH", "product_ndc": "79481-0201", "generic_name": "Sodium Fluoride", "labeler_name": "Meijer, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity Rinse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".2 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210714", "listing_expiration_date": "20271231"}