PreviDent 5000 Booster Plus Fruitastic
Colgate PreviDent 5000 ppm BOOSTERPLUS
Approved
Approval ID
83986c58-25ed-45a4-9d19-36f6ce32d76c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 1, 2023
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 Code0126-0072
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateJune 1, 2023
FDA Product Classification
INGREDIENTS (4)
SODIUM FLUORIDEActive
Quantity: 6 mg in 1 mL
Code: 8ZYQ1474W7
Classification: ACTIM
HYDRATED SILICAInactive
Code: Y6O7T4G8P9
Classification: IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDInactive
Code: K679OBS311
Classification: IACT
MICAInactive
Code: V8A1AW0880
Classification: IACT