Denti-Care Denti-Foam
10037-ST Strawberry Foam DentiCare Pro-Foam 2.72 % Topical Sodium Fluoride
Approved
Approval ID
1bc6f926-b304-4ca4-9ebf-06868782b4ec
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 22, 2023
Manufacturers
FDA
AMD Medicom Inc
DUNS: 256880576
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 Code64778-0379
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateDecember 22, 2023
FDA Product Classification
INGREDIENTS (1)
SODIUM FLUORIDEActive
Quantity: 0.0272 g in 1 g
Code: 8ZYQ1474W7
Classification: ACTIM