NDC Package 0699-0151-44 Topex 60 Second Fluoride Foam Spearmint

Sodium Fluoride Aerosol, Foam Dental - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0699-0151-44
Package Description:
1 CAN in 1 BOX / 125 g in 1 CAN
Product Code:
Proprietary Name:
Topex 60 Second Fluoride Foam Spearmint
Non-Proprietary Name:
Sodium Fluoride
Substance Name:
Sodium Fluoride
Usage Information:
Topex® Fluoride Foams are indicated for topical application to teeth to aid in the prevention of dental caries. The non-acidic nature of Neutral pH (NaF) is recommended for patients with ceramic or composite restorations.
11-Digit NDC Billing Format:
00699015144
NDC to RxNorm Crosswalk:
  • RxCUI: 1652849 - sodium fluoride 2.73 % Oral Foam
  • RxCUI: 1652849 - sodium fluoride 27.3 MG/ML Oral Foam
  • RxCUI: 1652849 - sodium fluoride 2.73 % (fluoride ion 1.23 % ) Oral Foam
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Dentsply Llc. Professional Division Trading As "sultan Healthcare"
    Dosage Form:
    Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
  • Active Ingredient(s):
    Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    01-01-1997
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0699-0151-44?

    The NDC Packaged Code 0699-0151-44 is assigned to a package of 1 can in 1 box / 125 g in 1 can of Topex 60 Second Fluoride Foam Spearmint, a human prescription drug labeled by Dentsply Llc. Professional Division Trading As "sultan Healthcare". The product's dosage form is aerosol, foam and is administered via dental form.

    Is NDC 0699-0151 included in the NDC Directory?

    Yes, Topex 60 Second Fluoride Foam Spearmint with product code 0699-0151 is active and included in the NDC Directory. The product was first marketed by Dentsply Llc. Professional Division Trading As "sultan Healthcare" on January 01, 1997 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0699-0151-44?

    The 11-digit format is 00699015144. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    4-4-20699-0151-445-4-200699-0151-44