1. Home
  2. Labeler Index
  3. Benard Industries Inc
  4. 55959-133
  5. NDC Package Code: 55959-133-01 Dolomax Cold Cough

NDC Package 55959-133-01 Dolomax Cold Cough

Acetaminophen,Dextromethorphan Hydrobromide,Guaifenesin,Phenylephrine Hydrochloride Tablet - 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:
55959-133-01
Package Description:
1 BLISTER PACK in 1 BOX / 12 TABLET in 1 BLISTER PACK
Product Code:
55959-133
Proprietary Name:
Dolomax Cold Cough
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
• do not take more than directed (see overdose warning)adults and children 12 years and over• take 2 tablets every 4 hours• swallow whole; do not crush, chew or dissolve• do not take more than 10 tablets in 24 hours children under 12 yearsask a doctor
11-Digit NDC Billing Format:
55959013301
NDC to RxNorm Crosswalk:
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Benard Industries Inc
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
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:
07-05-2021
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 55959-133-01?

The NDC Packaged Code 55959-133-01 is assigned to a package of 1 blister pack in 1 box / 12 tablet in 1 blister pack of Dolomax Cold Cough, a human over the counter drug labeled by Benard Industries Inc. The product's dosage form is tablet and is administered via oral form.

Is NDC 55959-133 included in the NDC Directory?

Yes, Dolomax Cold Cough with product code 55959-133 is active and included in the NDC Directory. The product was first marketed by Benard Industries Inc on July 05, 2021 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 55959-133-01?

The 11-digit format is 55959013301. 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
5-3-255959-133-015-4-255959-0133-01