NDC Package 41250-757-06 Mucus Relief Congestion And Headache Maximum Strength

Acetaminophen,Guaifenesin,Phenylephrine Hcl Liquid 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:
41250-757-06
Package Description:
177 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Mucus Relief Congestion And Headache Maximum Strength
Non-Proprietary Name:
Acetaminophen, Guaifenesin, Phenylephrine Hcl
Substance Name:
Acetaminophen; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed (see Overdose warning)do not take more than 6 doses in any 24-hour period measure only with dosing cup provided. Do not use any other dosing device.  keep dosing cup with products mL = milliliter  dose as follows or as directed by a doctor  adults and children 12 years and older: 20 mL in dosing cup provided every 4 hours children under 12 years of age: do not use
11-Digit NDC Billing Format:
41250075706
NDC to RxNorm Crosswalk:
  • RxCUI: 1116568 - acetaminophen 650 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
  • RxCUI: 1116568 - acetaminophen 32.5 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1116568 - acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG per 10 ML Oral Solution
  • RxCUI: 1116568 - acetaminophen 650 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1116568 - APAP 32.5 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Meijer, Inc.
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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:
    07-31-2018
    End Marketing Date:
    07-31-2025
    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 41250-757-06?

    The NDC Packaged Code 41250-757-06 is assigned to a package of 177 ml in 1 bottle, plastic of Mucus Relief Congestion And Headache Maximum Strength, a human over the counter drug labeled by Meijer, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 41250-757 included in the NDC Directory?

    Yes, Mucus Relief Congestion And Headache Maximum Strength with product code 41250-757 is active and included in the NDC Directory. The product was first marketed by Meijer, Inc. on July 31, 2018.

    What is the 11-digit format for NDC 41250-757-06?

    The 11-digit format is 41250075706. 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
    5-3-241250-757-065-4-241250-0757-06