NDC Package 47682-345-46 Mediqe Medi-mucus

Dextromethorphan Hbr,Guaifenesin Tablet 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:
47682-345-46
Package Description:
1 TABLET in 1 PACKET
Product Code:
Proprietary Name:
Mediqe Medi-mucus
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Adults and children:(12 years and older)Take 1 tablet every 4 hours with a full glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.Children under 12 yearsDo not use.
11-Digit NDC Billing Format:
47682034546
NDC to RxNorm Crosswalk:
  • RxCUI: 1147685 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral Tablet
  • RxCUI: 1147685 - dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral Tablet
  • RxCUI: 1147685 - guaifenesin 400 MG / dextromethorphan HBr 20 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Unifirst First Aid Corporation
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-03-2019
    End Marketing Date:
    07-01-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    47682-345-5050 PACKET in 1 BOX / 1 TABLET in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 47682-345-46?

    The NDC Packaged Code 47682-345-46 is assigned to a package of 1 tablet in 1 packet of Mediqe Medi-mucus, a human over the counter drug labeled by Unifirst First Aid Corporation. The product's dosage form is tablet and is administered via oral form.

    Is NDC 47682-345 included in the NDC Directory?

    Yes, Mediqe Medi-mucus with product code 47682-345 is active and included in the NDC Directory. The product was first marketed by Unifirst First Aid Corporation on June 03, 2019.

    What is the 11-digit format for NDC 47682-345-46?

    The 11-digit format is 47682034546. 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
    5-3-247682-345-465-4-247682-0345-46