Guaifenesin Dm Syrup
NDC Package 60687-817-17

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

Package Information

Guaifenesin Dm (guaifenesin and dextromethorphan) syrups is follow dosage below or use as directed by a physician.do not take more than 6 doses in any 24-hour period.Age (yr)Dose (mL)adults and children 12 years and over10 mL (2 teaspoonfuls) every 4 hourschildren 6 years to under 12 years5 mL (1 teaspoonful) every 4 hourschildren 2 years to under 6 years2.5 mL (1/2 teaspoonful) every 4 hourschildren under 2 yearsask a doctor. This formulation utilizes a syrup delivery system. Marketed by American Health Packaging, this product is identified by NDC 60687-817 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
60687-817-17
Package Description
10 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY (60687-817-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-817-40)
Product Code
60687-817
11-Digit Billing Format
60687081717
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution

Clinical Specifications

Proprietary Name
Guaifenesin Dm
Non-Proprietary Name
Guaifenesin And Dextromethorphan
Substance Name
Dextromethorphan; Guaifenesin
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Follow dosage below or use as directed by a physician.do not take more than 6 doses in any 24-hour period.Age (yr)Dose (mL)adults and children 12 years and over10 mL (2 teaspoonfuls) every 4 hourschildren 6 years to under 12 years5 mL (1 teaspoonful) every 4 hourschildren 2 years to under 6 years2.5 mL (1/2 teaspoonful) every 4 hourschildren under 2 yearsask a doctor

Regulatory & Marketing

Labeler Name
American Health Packaging
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-04-2024
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 60687-817-17 identifies a specific commercial package of 10 tray in 1 case / 10 cup, unit-dose in 1 tray (60687-817-46) / 5 ml in 1 cup, unit-dose (60687-817-40) of Guaifenesin Dm, a human over the counter drug labeled by American Health Packaging. This syrup is formulated for oral use and contains dextromethorphan; guaifenesin 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 American Health Packaging on August 04, 2024. The current certification is valid through December 31, 2026.

How is this American Health Packaging product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 60687081717. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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)
60687-817-17
11-Digit CMS (5-4-2)
60687-0817-17

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