anticavity
Generic: sodium fluoride
Labeler: amazon.com services llcDrug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
amazon.com services llc
Dosage Form
MOUTHWASH
Routes
Active Ingredients
sodium fluoride .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72288-439
Product ID
72288-439_4c20bcef-5513-c447-e063-6294a90a701b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2018-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72288439
Hyphenated Format
72288-439
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
- 473 mL in 1 BOTTLE, PLASTIC (72288-439-43)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c20bcef-5513-c447-e063-6294a90a701b", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["4a0220f8-748f-4a4a-9a8b-948756468f82"], "manufacturer_name": ["Amazon.com Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (72288-439-43)", "package_ndc": "72288-439-43", "marketing_start_date": "20180501"}], "brand_name": "Anticavity", "product_id": "72288-439_4c20bcef-5513-c447-e063-6294a90a701b", "dosage_form": "MOUTHWASH", "product_ndc": "72288-439", "generic_name": "Sodium fluoride", "labeler_name": "Amazon.com Services LLC", "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": "20180501", "listing_expiration_date": "20271231"}