Respiro-pro Liquid
NDC Package 71742-0010-1

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

Package Information

Respiro-pro (ammonium muriaticum, antimonium tartaricum, arsenicum album, bryonia (alba), calcarea carbonica, lobelia inflata, natrum sulphuricum, phosphorus, spongia tosta) liquids May temporarily relieve symptoms due to chronic lung disorders, lung inflammation. This formulation utilizes a liquid delivery system. Marketed by Guangzhou Renuma Medical Systems Co., Ltd, this product is identified by NDC 71742-0010.

Identification & Billing

NDC Package Code
71742-0010-1
Package Description
59 mL in 1 BOTTLE, DROPPER
Product Code
71742-0010
11-Digit Billing Format
71742001001

Clinical Specifications

Proprietary Name
Respiro-pro T016
Non-Proprietary Name
Ammonium Muriaticum, Antimonium Tartaricum, Arsenicum Album, Bryonia (alba), Calcarea Carbonica, Lobelia Inflata, Natrum Sulphuricum, Phosphorus, Spongia Tosta
Substance Name
Ammonium Chloride; Antimony Potassium Tartrate; Arsenic Trioxide; Bryonia Alba Root; Lobelia Inflata; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Sodium Sulfate; Spongia Officinalis Skeleton, Roasted
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)
Usage Information
May temporarily relieve symptoms due to chronic lung disorders, lung inflammation. May temporarily relieve symptoms due to chronic lung disorders, lung inflammation.

Regulatory & Marketing

Labeler Name
Guangzhou Renuma Medical Systems Co., Ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
10-26-2017
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 71742-0010-1 identifies a specific commercial package of 59 ml in 1 bottle, dropper of Respiro-pro T016, a human over the counter drug labeled by Guangzhou Renuma Medical Systems Co., Ltd. This liquid is formulated for oral use and contains ammonium chloride; antimony potassium tartrate; arsenic trioxide; bryonia alba root; lobelia inflata; oyster shell calcium carbonate, crude; phosphorus; sodium sulfate; spongia officinalis skeleton, roasted 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 Guangzhou Renuma Medical Systems Co., Ltd on October 26, 2017. The current certification is valid through December 31, 2026.

How is this Guangzhou Renuma Medical Systems Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71742001001. 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 (5-4-1)
71742-0010-1
11-Digit CMS (5-4-2)
71742-0010-01

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