anticavity
Generic: sodium fluoride
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
rite aid corporation
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
11822-5927
Product ID
11822-5927_499f2632-c7ab-9f52-e063-6294a90adaab
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2009-05-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118225927
Hyphenated Format
11822-5927
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 (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 (11822-5927-8)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "499f2632-c7ab-9f52-e063-6294a90adaab", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["1038904"], "spl_set_id": ["5a1b11f3-9d6f-4ac1-90f9-a95d4bb35589"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (11822-5927-8)", "package_ndc": "11822-5927-8", "marketing_start_date": "20090513"}], "brand_name": "Anticavity", "product_id": "11822-5927_499f2632-c7ab-9f52-e063-6294a90adaab", "dosage_form": "MOUTHWASH", "product_ndc": "11822-5927", "generic_name": "SODIUM FLUORIDE", "labeler_name": "Rite Aid Corporation", "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": "20090513", "listing_expiration_date": "20271231"}