Alpha-Pro
DTI APF - Strawberry
Approved
Approval ID
efe3646d-9eb1-4a49-aeb4-c4c224056851
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 11, 2017
Manufacturers
FDA
Dental Technologies, Inc.
DUNS: 148312838
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 Code55346-0942
Product Classification
G
Generic Name
Sodium Fluoride and Hydrofluoric Acid
Product Specifications
Route of AdministrationDENTAL
Effective DateDecember 11, 2017
FDA Product Classification
INGREDIENTS (2)
SODIUM FLUORIDEActive
Quantity: 7.9 mg in 1 g
Code: 8ZYQ1474W7
Classification: ACTIM
HYDROFLUORIC ACIDActive
Quantity: 4.4 mg in 1 g
Code: RGL5YE86CZ
Classification: ACTIM