Neutral Sodium Fluoride
Neutral Sodium Fluoride 0.2%
Approved
Approval ID
a4808e80-b8e0-4b18-b60c-9bdbb55dbef3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 28, 2013
Manufacturers
FDA
Sancilio & Company Inc
DUNS: 176681257
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sodium Fluoride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code44946-1050
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 28, 2013
FDA Product Classification
INGREDIENTS (8)
Sodium FluorideActive
Quantity: 20 mg in 1 mL
Code: 8ZYQ1474W7
Classification: ACTIM
WaterInactive
Code: 059QF0KO0R
Classification: IACT
GlycerinInactive
Code: PDC6A3C0OX
Classification: IACT
MethylparabenInactive
Code: A2I8C7HI9T
Classification: IACT
XylitolInactive
Code: VCQ006KQ1E
Classification: IACT
Propylene glycolInactive
Code: 6DC9Q167V3
Classification: IACT
SucraloseInactive
Code: 96K6UQ3ZD4
Classification: IACT
PropylparabenInactive
Code: Z8IX2SC1OH
Classification: IACT