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  5. NDC Package Code: 0031-8752-12 Robitussin Severe Multi-symptom Cough Cold Flu Nighttime

NDC Package 0031-8752-12 Robitussin Severe Multi-symptom Cough Cold Flu Nighttime

Acetaminophen,Diphenhydramine Hydrochloride,Phenylephrine Hydrochloride Solution Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
0031-8752-12
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code:
0031-8752
Proprietary Name:
Robitussin Severe Multi-symptom Cough Cold Flu Nighttime
Non-Proprietary Name:
Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride; Phenylephrine Hydrochloride
Usage Information:
•do not take more than 6 doses in any 24-hour period•do not exceed recommended dosage. Taking more than the recommended dose (overdose) may cause serious liver damage.•measure only with dosing cup provided•keep dosing cup with product•ml = milliliter•this adult product is not intended for use in children under 12 years of ageagedoseadults and children 12 years and over20 ml every 4 hourschildren under 12 yearsdo not use
11-Digit NDC Billing Format:
00031875212
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1375932 - acetaminophen 650 MG / diphenhydrAMINE HCl 25 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
  • RxCUI: 1375932 - acetaminophen 32.5 MG/ML / diphenhydramine hydrochloride 1.25 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1375932 - acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG per 10 ML Oral Solution
  • RxCUI: 1375932 - acetaminophen 650 MG / diphenhydramine HCl 25 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1375932 - APAP 32.5 MG/ML / Diphenhydramine Hydrochloride 1.25 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Haleon Us Holdings Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 650 mg/20mL
  • DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/20mL
  • PHENYLEPHRINE HYDROCHLORIDE 10 mg/20mL
    • Pharmacologic Class(es):
  • Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M0012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-01-2015
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0031-8752-181 BOTTLE in 1 CARTON / 237 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0031-8752-12?

    The NDC Packaged Code 0031-8752-12 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle of Robitussin Severe Multi-symptom Cough Cold Flu Nighttime, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is solution and is administered via oral form.

    Is NDC 0031-8752 included in the NDC Directory?

    Yes, Robitussin Severe Multi-symptom Cough Cold Flu Nighttime with product code 0031-8752 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on July 01, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0031-8752-12?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0031-8752-12?

    The 11-digit format is 00031875212. 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 4-4-2 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
    4-4-20031-8752-125-4-200031-8752-12