MedPath

PreviDent OrthoDefense

Colgate PreviDent 5000 ppm ORTHO DEFENSE™

Approved
Approval ID

99d37f3e-ac4f-4e8f-92e3-9b27d7632d35

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 13, 2022

Manufacturers
FDA

Colgate Oral Pharmaceuticals, Inc.

DUNS: 968801118

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 Code0126-0289
Product Classification
G
Generic Name
SODIUM FLUORIDE
Product Specifications
Route of AdministrationDENTAL
Effective DateJuly 13, 2022
FDA Product Classification

INGREDIENTS (16)

SODIUM FLUORIDEActive
Quantity: 6 mg in 1 mL
Code: 8ZYQ1474W7
Classification: ACTIM
FUMARIC ACIDInactive
Code: 88XHZ13131
Classification: IACT
SODIUM BENZOATEInactive
Code: OJ245FE5EU
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
POLOXAMER 338Inactive
Code: F75JV2T505
Classification: IACT
HYDRATED SILICAInactive
Code: Y6O7T4G8P9
Classification: IACT
POLYETHYLENE GLYCOL 600Inactive
Code: NL4J9F21N9
Classification: IACT
SACCHARIN SODIUMInactive
Code: SB8ZUX40TY
Classification: IACT
SORBITOLInactive
Code: 506T60A25R
Classification: IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDInactive
Code: K679OBS311
Classification: IACT
MICAInactive
Code: V8A1AW0880
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
TRICALCIUM PHOSPHATEInactive
Code: K4C08XP666
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
XANTHAN GUMInactive
Code: TTV12P4NEE
Classification: IACT

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PreviDent OrthoDefense - FDA Drug Approval Details