FluoriSHIELD
UNFLAVORED FluoriSHIELD BRAND OF 1.1% Sodium Fluoride Dental Gel
Approved
Approval ID
f6cb9fd1-f6fe-4c91-aded-0af6806822a9
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 11, 2011
Manufacturers
FDA
Medical Products Laboratories, Inc.
DUNS: 002290302
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 Code10733-130
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateFebruary 11, 2011
FDA Product Classification
INGREDIENTS (4)
SODIUM FLUORIDEActive
Quantity: 11 mg in 1 g
Code: 8ZYQ1474W7
Classification: ACTIB
HYDROXYETHYL CELLULOSE (4000 MPA.S FOR 1% AQUEOUS SOLUTION)Inactive
Code: ZYD53NBL45
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SACCHARIN SODIUMInactive
Code: SB8ZUX40TY
Classification: IACT