anticavity
Generic: sodium fluoride
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
rite aid corporation
Dosage Form
RINSE
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
11822-9718
Product ID
11822-9718_49da6529-c066-2253-e063-6294a90aea03
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2022-12-05
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118229718
Hyphenated Format
11822-9718
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
- .2 mg/mL
Packaging
- 1000 mL in 1 PACKAGE (11822-9718-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49da6529-c066-2253-e063-6294a90aea03", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["54a8b884-969a-4a41-ac2a-bc1f1fe9f7fe"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 PACKAGE (11822-9718-6)", "package_ndc": "11822-9718-6", "marketing_start_date": "20221205"}], "brand_name": "Anticavity", "product_id": "11822-9718_49da6529-c066-2253-e063-6294a90aea03", "dosage_form": "RINSE", "product_ndc": "11822-9718", "generic_name": "Sodium Fluoride", "labeler_name": "Rite Aid Corporation", "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": "20221205", "listing_expiration_date": "20271231"}