anticavity
Generic: sodium fluoride
Labeler: topco associates llcDrug Facts
Product Profile
Brand Name
anticavity
Generic Name
sodium fluoride
Labeler
topco associates llc
Dosage Form
RINSE
Routes
Active Ingredients
sodium fluoride .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
36800-971
Product ID
36800-971_4aba08c6-5e06-e60a-e063-6394a90abde8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2013-09-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
36800971
Hyphenated Format
36800-971
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 (36800-971-86)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4aba08c6-5e06-e60a-e063-6394a90abde8", "openfda": {"upc": ["0036800391512"], "unii": ["8ZYQ1474W7"], "rxcui": ["313029"], "spl_set_id": ["a9b8b2fe-0a60-4f65-b6f6-aae8509c919f"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (36800-971-86)", "package_ndc": "36800-971-86", "marketing_start_date": "20130919"}], "brand_name": "Anticavity", "product_id": "36800-971_4aba08c6-5e06-e60a-e063-6394a90abde8", "dosage_form": "RINSE", "product_ndc": "36800-971", "generic_name": "Sodium Fluoride", "labeler_name": "Topco Associates LLC", "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": "20130919", "listing_expiration_date": "20271231"}