PreviDent Alcohol Free
Colgate PreviDent Rinse
Approved
Approval ID
28e4f7cd-9fd8-4c7a-9e4b-d747fefc76c0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 11, 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 Code0126-0033
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateJuly 11, 2022
FDA Product Classification
INGREDIENTS (8)
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
SODIUM FLUORIDEActive
Quantity: 0.9 mg in 1 mL
Code: 8ZYQ1474W7
Classification: ACTIM
BENZOIC ACIDInactive
Code: 8SKN0B0MIM
Classification: IACT
POLOXAMER 338Inactive
Code: F75JV2T505
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
SODIUM BENZOATEInactive
Code: OJ245FE5EU
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT