1. Home
  2. Labeler Index
  3. Laboratorios Alfa
  4. 72483-101
  5. NDC Package Code: 72483-101-04 Resfridol Antitussive

NDC Package 72483-101-04 Resfridol Antitussive

Dextromethorphan Hbr,Guaifenesin Syrup 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:
72483-101-04
Package Description:
1 BOTTLE in 1 BOX / 120 mL in 1 BOTTLE
Product Code:
72483-101
Proprietary Name:
Resfridol Antitussive
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
■ only use the dosage cup provided■ shake well before use ■ do not exceed 6 doses per 24-hour period Age Dose adults and children 12 years and older 20 mL, every 4 hours children 6 to under 12 years 10 mL, every 4 hours children under 6 years do not use
11-Digit NDC Billing Format:
72483010104
NDC to RxNorm Crosswalk:
  • RxCUI: 2703096 - dextromethorphan HBr 5 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 2703096 - dextromethorphan hydrobromide 0.5 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 2703096 - dextromethorphan HBr 5 MG / guaifenesin 200 MG per 10 ML Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
Laboratorios Alfa
Dosage Form:
Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-31-2025
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.

Frequently Asked Questions

What is NDC 72483-101-04?

The NDC Packaged Code 72483-101-04 is assigned to a package of 1 bottle in 1 box / 120 ml in 1 bottle of Resfridol Antitussive, a human over the counter drug labeled by Laboratorios Alfa. The product's dosage form is syrup and is administered via oral form.

Is NDC 72483-101 included in the NDC Directory?

Yes, Resfridol Antitussive with product code 72483-101 is active and included in the NDC Directory. The product was first marketed by Laboratorios Alfa on January 31, 2025 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 11-digit format for NDC 72483-101-04?

The 11-digit format is 72483010104. 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
5-3-272483-101-045-4-272483-0101-04