firefly anticavity fluoride
Generic: sodium fluoride
Labeler: ranir llcDrug Facts
Product Profile
Brand Name
firefly anticavity fluoride
Generic Name
sodium fluoride
Labeler
ranir llc
Dosage Form
RINSE
Routes
Active Ingredients
sodium fluoride .5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
66923-007
Product ID
66923-007_081397d3-942f-4fe6-9d89-9338bdcbe8e2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2021-06-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66923007
Hyphenated Format
66923-007
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
firefly anticavity fluoride (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/mL
Packaging
- 473 mL in 1 BOTTLE (66923-007-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "081397d3-942f-4fe6-9d89-9338bdcbe8e2", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["9f98913f-6754-4e1c-98cf-b89fe87750f8"], "manufacturer_name": ["Ranir LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (66923-007-00)", "package_ndc": "66923-007-00", "marketing_start_date": "20210616"}], "brand_name": "Firefly Anticavity Fluoride", "product_id": "66923-007_081397d3-942f-4fe6-9d89-9338bdcbe8e2", "dosage_form": "RINSE", "product_ndc": "66923-007", "generic_name": "sodium fluoride", "labeler_name": "Ranir LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Firefly Anticavity Fluoride", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".5 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210616", "listing_expiration_date": "20261231"}