1. Home
  2. Labeler Index
  3. Ultradent Products, Inc.
  4. 51206-201
  5. NDC Package Code: 51206-201-02 Ultracare Oral Anesthetic Bubble Gum

NDC Package 51206-201-02 Ultracare Oral Anesthetic Bubble Gum

Benzocaine Gel Dental - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
51206-201-02
Package Description:
1 SYRINGE, PLASTIC in 1 BOX / 30 mL in 1 SYRINGE, PLASTIC
Product Code:
51206-201
Proprietary Name:
Ultracare Oral Anesthetic Bubble Gum
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Adults and children 2 years of age and olderApply a thin film to affected area. Allow to remain in place at least 1 minute and then spit out. Use up to 4 times daily or as directed by your dentist or doctor.Children between 2 and 12 years of ageShould be supervised in the use of this product.Children under 2 years of ageDo not use.
11-Digit NDC Billing Format:
51206020102
NDC to RxNorm Crosswalk:
  • RxCUI: 1045348 - Ultracare 20 % Oral Gel
  • RxCUI: 1045348 - benzocaine 0.2 MG/MG Oral Gel [Ultracare]
  • RxCUI: 1045348 - Ultracare 0.2 MG/MG Oral Gel
  • RxCUI: 1045348 - Ultracare 20 % Mucous Membrane Topical Gel
  • RxCUI: 238910 - benzocaine 20 % Oral Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Ultradent Products, Inc.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
    • Active Ingredient(s):
  • BENZOCAINE 200 mg/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    06-01-1986
    End Marketing Date:
    08-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 51206-201-02?

    The NDC Packaged Code 51206-201-02 is assigned to a package of 1 syringe, plastic in 1 box / 30 ml in 1 syringe, plastic of Ultracare Oral Anesthetic Bubble Gum, a human over the counter drug labeled by Ultradent Products, Inc.. The product's dosage form is gel and is administered via dental form.

    Is NDC 51206-201 included in the NDC Directory?

    Yes, Ultracare Oral Anesthetic Bubble Gum with product code 51206-201 is active and included in the NDC Directory. The product was first marketed by Ultradent Products, Inc. on June 01, 1986.

    What is the 11-digit format for NDC 51206-201-02?

    The 11-digit format is 51206020102. 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 5-3-2 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
    5-3-251206-201-025-4-251206-0201-02