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DOCTORS CHOICE

Approved
Approval ID

901f1d20-94e8-4931-9779-9fbbe40fdd5d

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 17, 2023

Manufacturers
FDA

Massco Dental A Division of Dunagin Pharmaceuticals

DUNS: 008081858

Products 2

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

STANOUS FLUORIDE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code63783-011
Product Classification
G
Generic Name
STANOUS FLUORIDE
Product Specifications
Route of AdministrationORAL
Effective DateDecember 17, 2023
FDA Product Classification

INGREDIENTS (4)

STANNOUS FLUORIDEActive
Quantity: 0.12 g in 120 g
Code: 3FTR44B32Q
Classification: ACTIM
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)Inactive
Code: S38J6RZN16
Classification: IACT
XYLITOLInactive
Code: VCQ006KQ1E
Classification: IACT

STANNOUS FLUORIDE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code63783-012
Product Classification
G
Generic Name
STANNOUS FLUORIDE
Product Specifications
Route of AdministrationORAL
Effective DateDecember 17, 2023
FDA Product Classification

INGREDIENTS (4)

STANNOUS FLUORIDEActive
Quantity: 0.12 g in 120 g
Code: 3FTR44B32Q
Classification: ACTIM
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)Inactive
Code: S38J6RZN16
Classification: IACT
XYLITOLInactive
Code: VCQ006KQ1E
Classification: IACT

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DOCTORS CHOICE - FDA Drug Approval Details