anticavity
Generic: sodium fluoride
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
cvs pharmacy, inc.
Dosage Form
RINSE
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59779-213
Product ID
59779-213_49dc3e9f-fa2b-d8dd-e063-6294a90a7f88
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2001-06-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59779213
Hyphenated Format
59779-213
Supplemental Identifiers
RxCUI
UPC
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 (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 (59779-213-44)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49dc3e9f-fa2b-d8dd-e063-6294a90a7f88", "openfda": {"upc": ["0050428415139"], "unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["a51357df-6d55-4030-a5db-42da7ba54a37"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "532 mL in 1 BOTTLE, PLASTIC (59779-213-44)", "package_ndc": "59779-213-44", "marketing_start_date": "20010619"}], "brand_name": "Anticavity", "product_id": "59779-213_49dc3e9f-fa2b-d8dd-e063-6294a90a7f88", "dosage_form": "RINSE", "product_ndc": "59779-213", "generic_name": "Sodium fluoride", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".2 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20010619", "listing_expiration_date": "20271231"}