Pro-chlo
NDC Package 66594-321-01

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Pro-chlo is do not exceed recommended dosage.Adults and children 12years of ageand over:2 teaspoonfuls (10 mL)every 6 hours, not toexceed 8 teaspoonfuls in24 hoursChildren 6 tounder 12 yearsof age:1 teaspoonful (5 mL)every 6 hours, not toexceed 4 teaspoonfuls in24 hoursChildren under6 years of age:Consult a doctor. Marketed by Pro-pharma, Llc, this product is identified by NDC 66594-321 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
66594-321-01
Package Description
30 mL in 1 BOTTLE
Product Code
66594-321
11-Digit Billing Format
66594032101
RxNorm Crosswalk
  • RxCUI: 1192685 - chlophedianol HCl 12.5 MG / phenylephrine HCl 5 MG / pyrilamine maleate 12.5 MG in 5 mL Oral Solution
  • RxCUI: 1192685 - chlophedianol hydrochloride 2.5 MG/ML / phenylephrine hydrochloride 1 MG/ML / pyrilamine maleate 2.5 MG/ML Oral Solution
  • RxCUI: 1192685 - chlophedianol hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG / pyrilamine maleate 12.5 MG per 5 ML Oral Solution

Clinical Specifications

Proprietary Name
Pro-chlo
Dosage Form
-
Usage Information
Do not exceed recommended dosage.Adults and children 12years of ageand over:2 teaspoonfuls (10 mL)every 6 hours, not toexceed 8 teaspoonfuls in24 hoursChildren 6 tounder 12 yearsof age:1 teaspoonful (5 mL)every 6 hours, not toexceed 4 teaspoonfuls in24 hoursChildren under6 years of age:Consult a doctor.

Regulatory & Marketing

Labeler Name
Pro-pharma, Llc
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-12-2011
Listing Expiration
12-31-2017
Exclude Flag
I
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 (66594-321). Click a package code to view its specific billing and regulatory data.

66594-321-16
473 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 66594-321-01 identifies a specific commercial package of 30 ml in 1 bottle of Pro-chlo, labeled by Pro-pharma, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Pro-pharma, Llc on December 12, 2011. The current certification is valid through December 31, 2017.

How is this Pro-pharma, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 66594032101. 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)
66594-321-01
11-Digit CMS (5-4-2)
66594-0321-01

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