anticavity fluoride rinse
Generic: sodium fluoride
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
anticavity fluoride rinse
Generic Name
sodium fluoride
Labeler
cvs pharmacy, inc.
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59779-163
Product ID
59779-163_4a9333a3-a8d6-0dcd-e063-6294a90afdab
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2008-09-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59779163
Hyphenated Format
59779-163
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 fluoride rinse (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/mL
Packaging
- 1000 mL in 1 PACKAGE (59779-163-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a9333a3-a8d6-0dcd-e063-6294a90afdab", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1038904"], "spl_set_id": ["b2f7490c-e2af-49df-b054-70fb4815f729"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 PACKAGE (59779-163-86)", "package_ndc": "59779-163-86", "marketing_start_date": "20080915"}], "brand_name": "Anticavity Fluoride Rinse", "product_id": "59779-163_4a9333a3-a8d6-0dcd-e063-6294a90afdab", "dosage_form": "MOUTHWASH", "product_ndc": "59779-163", "generic_name": "Sodium Fluoride", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity Fluoride Rinse", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080915", "listing_expiration_date": "20271231"}