Lungs And Bronchial Relief Liquid
NDC Package 57955-9991-2
Package Information
Lungs And Bronchial Relief (ammonium carbonicum, antimonium arsenicicum, antimonium tartaricum, arsenicum album, bromium, carbo vegetabilis, chlorinum, kali carbonicum, lobelia inflata, stannum metallicum, sulphuricum acidum.) liquids is uses † for temporary relief of minor symptomsof difficult breathing:lung congestionbronchial inflammationwheezinghoarsenesscoughing attacksbronchial mucusmucous congestion† Claims based on traditional Homeopathic practice, not accepted medical evidence, notFDA evaluated. This formulation utilizes a liquid delivery system. Marketed by King Bio Inc., this product is identified by NDC 57955-9991.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 10 [hp_X]/59mL
- AMMONIUM CARBONATE 10 [hp_X]/59mL
- ANTIMONY ARSENATE 10 [hp_X]/59mL
- ANTIMONY POTASSIUM TARTRATE 10 [hp_X]/59mL
- ARSENIC TRIOXIDE 10 [hp_X]/59mL
- BROMINE 10 [hp_X]/59mL
- CHLORINE 10 [hp_X]/59mL
- LOBELIA INFLATA WHOLE 10 [hp_X]/59mL
- POTASSIUM CARBONATE 10 [hp_X]/59mL
- SULFURIC ACID 10 [hp_X]/59mL
- TIN 10 [hp_X]/59mL
Regulatory & Marketing
Hierarchy Structure
- 57955 - King Bio Inc.
- 57955-9991 - Lungs And Bronchial Relief
- 57955-9991-2 - 59 mL in 1 BOTTLE, SPRAY
- 57955-9991 - Lungs And Bronchial Relief
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 57955-9991-2 identifies a specific commercial package of 59 ml in 1 bottle, spray of Lungs And Bronchial Relief, a human over the counter drug labeled by King Bio Inc.. This liquid is formulated for oral use and contains activated charcoal; ammonium carbonate; antimony arsenate; antimony potassium tartrate; arsenic trioxide; bromine; chlorine; lobelia inflata whole; potassium carbonate; sulfuric acid; tin 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 King Bio Inc. on October 20, 2025. The current certification is valid through December 31, 2027.
How is this King Bio Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 57955999102. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.