NDC Package 67172-022-18 Chloraseptic

Menthol And Benzocaine Lozenge Oral - 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:
67172-022-18
Package Description:
3 BLISTER PACK in 1 CARTON / 6 LOZENGE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Chloraseptic
Non-Proprietary Name:
Menthol And Benzocaine
Substance Name:
Benzocaine; Menthol
Usage Information:
Adults and children 6 years of age and older: Take 1 lozenge every 2 hours as needed. Allow lozenges to dissolve slowly in the mouth.Children under 6 years of age: Do not use.
11-Digit NDC Billing Format:
67172002218
NDC to RxNorm Crosswalk:
  • RxCUI: 308668 - benzocaine 6 MG / menthol 10 MG Oral Lozenge
  • RxCUI: 802559 - Chloraseptic Sore Throat 10 MG / 6 MG Oral Lozenge
  • RxCUI: 802559 - benzocaine 6 MG / menthol 10 MG Oral Lozenge [Chloraseptic Sore Throat]
  • RxCUI: 802559 - Chloraseptic Sore Throat (benzocaine 6 MG / menthol 10 MG) Oral Lozenge
  • RxCUI: 802559 - Chloraseptic Sore Throat Oral Lozenge
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Prestige Brands Holdings, Inc.
    Dosage Form:
    Lozenge - A solid preparation containing one or more medicaments, usually in a flavored, sweetened base which is intended to dissolve or disintegrate slowly in the mouth. A lollipop is a lozenge on a stick.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    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:
    08-01-2010
    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 67172-022-18?

    The NDC Packaged Code 67172-022-18 is assigned to a package of 3 blister pack in 1 carton / 6 lozenge in 1 blister pack of Chloraseptic, a human over the counter drug labeled by Prestige Brands Holdings, Inc.. The product's dosage form is lozenge and is administered via oral form.

    Is NDC 67172-022 included in the NDC Directory?

    Yes, Chloraseptic with product code 67172-022 is active and included in the NDC Directory. The product was first marketed by Prestige Brands Holdings, Inc. on August 01, 2010 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 67172-022-18?

    The 11-digit format is 67172002218. 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
    5-3-267172-022-185-4-267172-0022-18