Lung Distress Spray
NDC Package 50845-0275-2
Package Information
Lung Distress (blatta orientalis, bryonia (alba), carbo vegetabilis, eupatorium perfoliatum, histaminum hydrochloricum, iodium, ipecacuanha, lung suis, natrum sulphuricum, nitricum acidum, pulsatilla (pratensis), quebracho, sambucus nigra, sticta pulmonaria, urtica urens) sprays is adults and children over 12: Spray twice under the tongue 3 times per day. This formulation utilizes a spray delivery system. Marketed by Liddell Laboratories, this product is identified by NDC 50845-0275.
Identification & Billing
Clinical Specifications
- BLATTA ORIENTALIS 12 [hp_X]/mL
- BRYONIA ALBA ROOT 12 [hp_X]/mL
- ACTIVATED CHARCOAL 30 [hp_C]/mL
- EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X]/mL
- HISTAMINE DIHYDROCHLORIDE 6 [hp_X]/mL
- IODINE 200 [hp_C]/mL
- IPECAC 200 [hp_C]/mL
- SUS SCROFA LUNG 4 [hp_X]/mL
- SODIUM SULFATE 200 [hp_C]/mL
- NITRIC ACID 200 [hp_C]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_C]/mL
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK 3 [hp_X]/mL
- SAMBUCUS NIGRA FLOWERING TOP 30 [hp_C]/mL
- LOBARIA PULMONARIA 6 [hp_X]/mL
- URTICA URENS WHOLE 6 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 50845 - Liddell Laboratories
- 50845-0275 - Lung Distress
- 50845-0275-2 - 1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY (50845-0275-1)
- 50845-0275 - Lung Distress
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 50845-0275-2 identifies a specific commercial package of 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray (50845-0275-1) of Lung Distress, a human over the counter drug labeled by Liddell Laboratories. This spray is formulated for oral use and contains blatta orientalis; bryonia alba root; activated charcoal; eupatorium perfoliatum flowering top; histamine dihydrochloride; iodine; ipecac; sus scrofa lung; sodium sulfate; nitric acid; pulsatilla pratensis whole; aspidosperma quebracho-blanco bark; sambucus nigra flowering top; lobaria pulmonaria; urtica urens whole 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 Liddell Laboratories on October 05, 2021. The current certification is valid through December 31, 2026.
How is this Liddell Laboratories product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845027502. 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.