Denti-Care
Denti-Care Denti-Foam 1.76% Topical Sodium Fluoride Foam Strawberry
Approved
Approval ID
8fb3042c-09d7-4001-90cf-1e33a4d9ae13
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 6, 2011
Manufacturers
FDA
AR Medicom Inc
DUNS: 247876295
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 Code64778-1379
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateFebruary 6, 2011
FDA Product Classification
INGREDIENTS (2)
sodium fluorideActive
Quantity: .0176 g in 1 g
Code: 8ZYQ1474W7
Classification: ACTIB
HYDROFLUORIC ACIDActive
Quantity: 0.010 g in 1 g
Code: RGL5YE86CZ
Classification: ACTIB