NDC Package 67234-048-01 Kendra Skin Protection And Pain Relief For Hair Removal

Lanolin,Petrolatum And Lidocaine Kit - 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:
67234-048-01
Package Description:
1 KIT in 1 CARTON * 28 g in 1 TUBE * 28 g in 1 TUBE
Product Code:
Proprietary Name:
Kendra Skin Protection And Pain Relief For Hair Removal
Non-Proprietary Name:
Lanolin, Petrolatum And Lidocaine
Usage Information:
After procedure, apply A&D Skin Protectant as needed to affected skin. For adult use only.Before procedure, apply a small amount of pain relieving cream to affected area, and allow to dry. Application may be repeated up to 4 times daily.
11-Digit NDC Billing Format:
67234004801
NDC to RxNorm Crosswalk:
  • RxCUI: 1421893 - lidocaine 4 % Topical Cream
  • RxCUI: 1421893 - lidocaine 40 MG/ML Topical Cream
  • RxCUI: 664981 - lanolin 15.5 % / petrolatum 53.4 % Topical Ointment
  • RxCUI: 664981 - lanolin 0.155 MG/MG / petrolatum 0.534 MG/MG Topical Ointment
  • RxCUI: 664981 - lanolin 15.5 GM per 100 GM / petrolatum 53.4 GM per 100 GM Topical Ointment
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Natureplex, Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    part347
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-04-2003
    Listing Expiration Date:
    12-31-2024
    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 67234-048-01?

    The NDC Packaged Code 67234-048-01 is assigned to a package of 1 kit in 1 carton * 28 g in 1 tube * 28 g in 1 tube of Kendra Skin Protection And Pain Relief For Hair Removal, a human over the counter drug labeled by Natureplex, Llc. The product's dosage form is kit and is administered via form.

    Is NDC 67234-048 included in the NDC Directory?

    Yes, Kendra Skin Protection And Pain Relief For Hair Removal with product code 67234-048 is active and included in the NDC Directory. The product was first marketed by Natureplex, Llc on June 04, 2003 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67234-048-01?

    The 11-digit format is 67234004801. 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
    5-3-267234-048-015-4-267234-0048-01