Lung Large Intestine Meridian Opener Liquid
NDC Package 43742-0811-1
Package Information
Lung Large Intestine Meridian Opener (aloe, alumina, apis mellifica, arsenicum album, baryta carbonica, bryonia (alba), carbo vegetabilis, chamomilla, kali bichromicum, phosphorus, plumbum metallicum, pyrogenium, sulphur) liquids is for temporary relief of tickling cough, hoarseness, hay fever, headache, eye pain, constipation, indigestion and diarrhea.****These statements are based upon traditional homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc, this product is identified by NDC 43742-0811.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 30 [hp_C]/mL
- ALOE VERA LEAF 30 [hp_C]/mL
- ALUMINUM OXIDE 30 [kp_C]/mL
- APIS MELLIFERA 30 [hp_C]/mL
- ARSENIC TRIOXIDE 30 [hp_C]/mL
- BARIUM CARBONATE 30 [hp_C]/mL
- BRYONIA ALBA ROOT 30 [hp_C]/mL
- LEAD 30 [hp_C]/mL
- MATRICARIA CHAMOMILLA WHOLE 30 [hp_C]/mL
- PHOSPHORUS 30 [hp_C]/mL
- POTASSIUM DICHROMATE 30 [hp_C]/mL
- RANCID BEEF 30 [hp_C]/mL
- SULFUR 30 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc
- 43742-0811 - Lung Large Intestine Meridian Opener
- 43742-0811-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-0811 - Lung Large Intestine Meridian Opener
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 43742-0811-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Lung Large Intestine Meridian Opener, a human over the counter drug labeled by Deseret Biologicals, Inc. This liquid is formulated for oral use and contains activated charcoal; aloe vera leaf; aluminum oxide; apis mellifera; arsenic trioxide; barium carbonate; bryonia alba root; lead; matricaria chamomilla whole; phosphorus; potassium dichromate; rancid beef; sulfur 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 Deseret Biologicals, Inc on July 13, 2016. The current certification is valid through December 31, 2026.
How is this Deseret Biologicals, Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742081101. 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.