NDC Package 49035-165-09 Severe Congestion Relief Maximum Strength Sinus

Acetaminophen,Guaifenesin,Phenylephrine Hcl Tablet, Film 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:
49035-165-09
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Severe Congestion Relief Maximum Strength Sinus
Non-Proprietary Name:
Acetaminophen, Guaifenesin, Phenylephrine Hcl
Substance Name:
Acetaminophen; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed do not take more than 12 caplets in any 24-hour periodadults and children 12 years and over: take 2 caplets every 4 hours children under 12 years of age: do not use
11-Digit NDC Billing Format:
49035016509
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:
    Wal-mart Stores Inc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-30-2014
    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 49035-165-09?

    The NDC Packaged Code 49035-165-09 is assigned to a package of 2 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack of Severe Congestion Relief Maximum Strength Sinus, a human over the counter drug labeled by Wal-mart Stores Inc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 49035-165 included in the NDC Directory?

    Yes, Severe Congestion Relief Maximum Strength Sinus with product code 49035-165 is active and included in the NDC Directory. The product was first marketed by Wal-mart Stores Inc on June 30, 2014 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 49035-165-09?

    The 11-digit format is 49035016509. 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
    5-3-249035-165-095-4-249035-0165-09