NDC Package 63940-337-02 Severe Congestion

Acetaminophen,Guaifenesin,And Phenylephrine Hydrochloride Tablet, Coated 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:
63940-337-02
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET, COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Severe Congestion
Non-Proprietary Name:
Acetaminophen, Guaifenesin, And Phenylephrine Hydrochloride
Substance Name:
Acetaminophen; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed (see Overdose warning) do not take more than 12 caplets in any 24-hour periodadults and children 12 years and older:  take 2 caplets every 4 hourschildren under 12 years of age:  do not use
11-Digit NDC Billing Format:
63940033702
NDC to RxNorm Crosswalk:
  • RxCUI: 1243679 - acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1243679 - acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - APAP 325 MG / GG 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1243679 - APAP 325 MG / Guaifenesin 200 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Harmon Stores Inc.
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    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:
    09-11-2018
    End Marketing 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 63940-337-02?

    The NDC Packaged Code 63940-337-02 is assigned to a package of 2 blister pack in 1 carton / 10 tablet, coated in 1 blister pack of Severe Congestion, a human over the counter drug labeled by Harmon Stores Inc.. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 63940-337 included in the NDC Directory?

    Yes, Severe Congestion with product code 63940-337 is active and included in the NDC Directory. The product was first marketed by Harmon Stores Inc. on September 11, 2018.

    What is the 11-digit format for NDC 63940-337-02?

    The 11-digit format is 63940033702. 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
    5-3-263940-337-025-4-263940-0337-02