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  5. NDC Package Code: 41163-432-67 Equaline Nasal Decongestant Non Drowsy Maximum Strength

NDC Package 41163-432-67 Equaline Nasal Decongestant Non Drowsy Maximum Strength

Pseudoephedrine Hcl Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
41163-432-67
Package Description:
8 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
41163-432
Proprietary Name:
Equaline Nasal Decongestant Non Drowsy Maximum Strength
Non-Proprietary Name:
Pseudoephedrine Hcl
Substance Name:
Pseudoephedrine Hydrochloride
Usage Information:
Pseudoephedrine is used for the temporary relief of stuffy nose and sinus pain/pressure caused by infection (such as the common cold, flu) or other breathing illnesses (such as hay fever, allergies, bronchitis). Pseudoephedrine is a decongestant (sympathomimetic). It works by narrowing the blood vessels to decrease swelling and congestion. If you are self-treating with this medication, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions section.) Cough-and-cold products have not been shown to be safe or effective in children younger than 6 years. Long-acting tablets/capsules are not recommended for use in children younger than 12 years. Do not use this pseudoephedrine product in children younger than 12 years unless specifically directed by the doctor. Ask your doctor or pharmacist for more details about using your product safely. These products do not cure or shorten the length of the common cold and may cause serious side effects. To decrease the risk for serious side effects, carefully follow all dosage directions. Do not use this product to make a child sleepy. Do not give other cough-and-cold medication that might contain the same or similar ingredients (see also Drug Interactions section). Ask the doctor or pharmacist about other ways to relieve cough and cold symptoms (such as drinking enough fluids, using a humidifier or saline nose drops/spray).
11-Digit NDC Billing Format:
41163043267
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
8 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1049160 - pseudoephedrine HCl 30 MG Oral Tablet
  • RxCUI: 1049160 - pseudoephedrine hydrochloride 30 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    United Natural Foods, Inc. Dba Unfi
    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.
    • Active Ingredient(s):
  • PSEUDOEPHEDRINE HYDROCHLORIDE 30 mg/1
    • Pharmacologic Class(es):
  • Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
  • alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • 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:
    08-17-2004
    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 41163-432-67?

    The NDC Packaged Code 41163-432-67 is assigned to a package of 8 blister pack in 1 carton / 6 tablet, film coated in 1 blister pack of Equaline Nasal Decongestant Non Drowsy Maximum Strength, a human over the counter drug labeled by United Natural Foods, Inc. Dba Unfi. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 8 billable units per package.

    Is NDC 41163-432 included in the NDC Directory?

    Yes, Equaline Nasal Decongestant Non Drowsy Maximum Strength with product code 41163-432 is active and included in the NDC Directory. The product was first marketed by United Natural Foods, Inc. Dba Unfi on August 17, 2004 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 41163-432-67?

    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 8.

    What is the 11-digit format for NDC 41163-432-67?

    The 11-digit format is 41163043267. 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
    5-3-241163-432-675-4-241163-0432-67