NDC Package 41250-706-21 Oral Analgesic Maximum Strength

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
41250-706-21
Package Description:
1 TUBE in 1 CARTON / 6 g in 1 TUBE
Product Code:
Proprietary Name:
Oral Analgesic Maximum Strength
Usage Information:
Directions    remove cap and cut tip of the tube on score markadults and children 2 years of age and over:  apply to tyhe affected area up to 4 times daily or as directed by doctor/dentistchildren under 12 years of age: should be supervised in the use of this productChildren under 2 years of age:  ask a doctor/dentistOther informationDo not use if tube tip is cut prior to opening.Inactive ingredients cellulose gum, gelatin, methyl salicylate, pectin, plasticized hydrdocarbon gel, polyethylene glycol, sodium saccharin
11-Digit NDC Billing Format:
41250070621
NDC to RxNorm Crosswalk:
  • RxCUI: 1045344 - benzocaine 20 % / menthol 0.25 % Oral Paste
  • RxCUI: 1045344 - benzocaine 0.2 MG/MG / menthol 0.0025 MG/MG Oral Paste
  • RxCUI: 1045344 - benzocaine 0.2 MG/MG / menthol 0.0025 MG/MG Mucous Membrane Topical Paste
  • RxCUI: 1045344 - benzocaine 20 % / menthol 0.25 % Mucous Membrane Topical Paste
  • Labeler Name:
    Meijer Distribution Inc.
    Sample Package:
    No
    Start Marketing Date:
    05-13-2010
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    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 41250-706-21?

    The NDC Packaged Code 41250-706-21 is assigned to a package of 1 tube in 1 carton / 6 g in 1 tube of Oral Analgesic Maximum Strength, labeled by Meijer Distribution Inc.. The product's dosage form is and is administered via form.

    Is NDC 41250-706 included in the NDC Directory?

    No, Oral Analgesic Maximum Strength with product code 41250-706 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Meijer Distribution Inc. on May 13, 2010 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 41250-706-21?

    The 11-digit format is 41250070621. 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
    5-3-241250-706-215-4-241250-0706-21