anticavity
Generic: sodium fluoride
Labeler: demoulas super markets, incDrug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
demoulas super markets, inc
Dosage Form
RINSE
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
53942-971
Product ID
53942-971_49f11bf5-6924-cc6e-e063-6394a90a9459
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2022-04-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53942971
Hyphenated Format
53942-971
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
- .1 mg/mL
Packaging
- 1000 mL in 1 BOTTLE, PLASTIC (53942-971-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49f11bf5-6924-cc6e-e063-6394a90a9459", "openfda": {"upc": ["0049705790434"], "unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["096e6a1d-316b-432a-bf27-70e8a13337cc"], "manufacturer_name": ["Demoulas Super Markets, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (53942-971-86)", "package_ndc": "53942-971-86", "marketing_start_date": "20220404"}], "brand_name": "Anticavity", "product_id": "53942-971_49f11bf5-6924-cc6e-e063-6394a90a9459", "dosage_form": "RINSE", "product_ndc": "53942-971", "generic_name": "Sodium Fluoride", "labeler_name": "Demoulas Super Markets, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anticavity", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".1 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220404", "listing_expiration_date": "20271231"}