Emf Spray
NDC Package 50845-0248-1
Package Information
Emf (argentum nitricum, arnica montana, baptisia tinctoria, cinchona officinalis, galium aparine, hepar suis, natrum carbonicum, panax ginseng, phosphoricum acidum, phosphorus, rhododendron chrysanthum, strontium carbonicum, sulphur iodatum, thuja occidentalis, x-ray) sprays is adults and children over 12: Spray twice under the tongue three times per day for one month. This formulation utilizes a spray delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0248.
Identification & Billing
Clinical Specifications
- SILVER NITRATE 200 [hp_C]/mL
- ARNICA MONTANA WHOLE 3 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 1 [hp_X]/mL
- CINCHONA OFFICINALIS BARK 3 [hp_X]/mL
- GALIUM APARINE WHOLE 6 [hp_X]/mL
- PORK LIVER 3 [hp_X]/mL
- SODIUM CARBONATE 3 [hp_X]/mL
- ASIAN GINSENG 12 [hp_X]/mL
- PHOSPHORIC ACID 6 [hp_X]/mL
- PHOSPHORUS 30 [hp_C]/mL
- RHODODENDRON AUREUM LEAF 30 [hp_C]/mL
- STRONTIUM CARBONATE 200 [hp_C]/mL
- SULFUR IODIDE 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 200 [hp_C]/mL
- ALCOHOL, X-RAY EXPOSED (1000 RAD) 200 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 50845 - Liddell Laboratories, Inc.
- 50845-0248 - Emf
- 50845-0248-1 - 30 mL in 1 BOTTLE, SPRAY
- 50845-0248 - Emf
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 50845-0248-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Emf, a human over the counter drug labeled by Liddell Laboratories, Inc.. This spray is formulated for oral use and contains silver nitrate; arnica montana whole; baptisia tinctoria root; cinchona officinalis bark; galium aparine whole; pork liver; sodium carbonate; asian ginseng; phosphoric acid; phosphorus; rhododendron aureum leaf; strontium carbonate; sulfur iodide; thuja occidentalis leafy twig; alcohol, x-ray exposed (1000 rad) 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, Inc. on January 30, 2019. The current certification is valid through December 31, 2026.
How is this Liddell Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845024801. 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.