Perfect Choice
APF Gel - Vanilla Orange
Approved
Approval ID
3b2d5edc-ddc2-4c91-aeba-9ba982c7793e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 22, 2018
Manufacturers
FDA
Young Dental Manufacturing Co 1, LLC.
DUNS: 006309355
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sodium Fluoride and Hydrofluoric Acid
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0273-7003
Product Classification
G
Generic Name
Sodium Fluoride and Hydrofluoric Acid
Product Specifications
Route of AdministrationDENTAL
Effective DateDecember 22, 2018
FDA Product Classification
INGREDIENTS (2)
HYDROFLUORIC ACIDActive
Quantity: 4.4 mg in 1 g
Code: RGL5YE86CZ
Classification: ACTIM
SODIUM FLUORIDEActive
Quantity: 7.9 mg in 1 g
Code: 8ZYQ1474W7
Classification: ACTIM