Chlo Tuss Liquid
NDC Package 12830-762-16

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Chlo Tuss (chlophedianol hydrochloride, dexbrompheniramine maleate, pseudoephedrine hydrochloride) liquids is do not exceed recommended dosage.  Adults and children12 years of age and over:2 teaspoonfuls (10 mL)every 6 hours, not toexceed 8 teaspoonfulsin 24 hours Children 6 to under12 years of age: 1 teaspoonful (5 mL)every 6 hours, not toexceed 4 teaspoonfulsin 24 hours Children under6 years of age: Consult a doctor  . This formulation utilizes a liquid delivery system. Marketed by R.a. Mcneil Company, this product is identified by NDC 12830-762 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
12830-762-16
Package Description
473 mL in 1 BOTTLE
Product Code
12830-762
11-Digit Billing Format
12830076216
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
473 ML
RxNorm Crosswalk
  • RxCUI: 1441376 - chlophedianol HCl 12.5 MG / dexbrompheniramine maleate 1 MG / pseudoephedrine HCl 30 MG in 5 mL Oral Solution
  • RxCUI: 1441376 - chlophedianol hydrochloride 2.5 MG/ML / dexbrompheniramine maleate 0.2 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Solution
  • RxCUI: 1441376 - chlophedianol HCl 12.5 MG / dexbrompheniramine maleate 1 MG / pseudoephedrine HCl 30 MG per 5 ML Oral Solution
  • RxCUI: 1441376 - chlophedianol HCl 25 MG / dexbrompheniramine maleate 2 MG / pseudoephedrine HCl 60 MG per 10 ML Oral Solution
  • RxCUI: 1441376 - chlophedianol HCl 6.25 MG / dexbrompheniramine maleate 0.5 MG / pseudoephedrine HCl 15 MG per 2.5 ML Oral Solution

Clinical Specifications

Proprietary Name
Chlo Tuss
Non-Proprietary Name
Chlophedianol Hydrochloride, Dexbrompheniramine Maleate, Pseudoephedrine Hydrochloride
Substance Name
Chlophedianol Hydrochloride; Dexbrompheniramine Maleate; Pseudoephedrine Hydrochloride
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not exceed recommended dosage.  Adults and children12 years of age and over:2 teaspoonfuls (10 mL)every 6 hours, not toexceed 8 teaspoonfulsin 24 hours Children 6 to under12 years of age: 1 teaspoonful (5 mL)every 6 hours, not toexceed 4 teaspoonfulsin 24 hours Children under6 years of age: Consult a doctor  

Regulatory & Marketing

Labeler Name
R.a. Mcneil Company
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-01-2013
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (12830-762). Click a package code to view its specific billing and regulatory data.

12830-762-15
15 mL in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 12830-762-16 identifies a specific commercial package of 473 ml in 1 bottle of Chlo Tuss, a human over the counter drug labeled by R.a. Mcneil Company. This liquid is formulated for oral use and contains chlophedianol hydrochloride; dexbrompheniramine maleate; pseudoephedrine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by R.a. Mcneil Company on October 01, 2013. The current certification is valid through December 31, 2026.

How is this R.a. Mcneil Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 12830076216. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 473 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
12830-762-16
11-Digit CMS (5-4-2)
12830-0762-16

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.