NEUTRA MAXX 5000
Approved
Approval ID
fcbe6baa-2827-49df-9316-42cc86595203
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 17, 2023
Manufacturers
FDA
Massco Dental A Division of Dunagin Pharmaceuticals
DUNS: 008081858
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 Code63783-504
Product Classification
G
Generic Name
SODIUM FLUORIDE
Product Specifications
Route of AdministrationORAL
Effective DateDecember 17, 2023
FDA Product Classification
INGREDIENTS (8)
SACCHARIN SODIUMInactive
Code: SB8ZUX40TY
Classification: IACT
SODIUM FLUORIDEActive
Quantity: 1.428 g in 120 g
Code: 8ZYQ1474W7
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
XYLITOLInactive
Code: VCQ006KQ1E
Classification: IACT
POTASSIUM NITRATEInactive
Code: RU45X2JN0Z
Classification: IACT
CARBOXYMETHYLCELLULOSE SODIUMInactive
Code: K679OBS311
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
SODIUM PHOSPHATEInactive
Code: SE337SVY37
Classification: IACT