NDC Package 46122-700-71 Gnp Mucus Relief PE

Guaifenesin/phenylephrine 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:
46122-700-71
Package Description:
1 BOTTLE in 1 CARTON / 50 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Gnp Mucus Relief PE
Non-Proprietary Name:
Guaifenesin/phenylephrine
Substance Name:
Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Adults and children 12 years and over: take 1 caplet every 4 hours as neededchildren 6 to under 12 years: take 1/2 caplet every 4 hours as neededchildren under 6 years: consult a doctorDo not exceed 6 doses in a 24 hour period or as directed by a doctor.
11-Digit NDC Billing Format:
46122070071
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1304111 - guaiFENesin 400 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1304111 - guaifenesin 400 MG / phenylephrine hydrochloride 10 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Amerisourcebergen Drug Corp
    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:
    01-13-2022
    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 46122-700-71?

    The NDC Packaged Code 46122-700-71 is assigned to a package of 1 bottle in 1 carton / 50 tablet in 1 bottle of Gnp Mucus Relief PE, a human over the counter drug labeled by Amerisourcebergen Drug Corp. The product's dosage form is tablet and is administered via oral form.

    Is NDC 46122-700 included in the NDC Directory?

    Yes, Gnp Mucus Relief PE with product code 46122-700 is active and included in the NDC Directory. The product was first marketed by Amerisourcebergen Drug Corp on January 13, 2022 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 NDC billing unit for package 46122-700-71?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 46122-700-71?

    The 11-digit format is 46122070071. 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
    5-3-246122-700-715-4-246122-0700-71