anticavity
Generic: sodium fluoride
Labeler: target corporationDrug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
target corporation
Dosage Form
RINSE
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
11673-004
Product ID
11673-004_4b1dd4df-4c3d-c4fb-e063-6294a90a25e0
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2011-08-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673004
Hyphenated Format
11673-004
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
- 500 mL in 1 BOTTLE, PLASTIC (11673-004-77)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b1dd4df-4c3d-c4fb-e063-6294a90a25e0", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["abfc1973-60ab-44e5-8147-33739d8bd7a3"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (11673-004-77)", "package_ndc": "11673-004-77", "marketing_start_date": "20110826"}], "brand_name": "Anticavity", "product_id": "11673-004_4b1dd4df-4c3d-c4fb-e063-6294a90a25e0", "dosage_form": "RINSE", "product_ndc": "11673-004", "generic_name": "Sodium fluoride", "labeler_name": "Target 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": "20110826", "listing_expiration_date": "20271231"}