Vaccines Liquid
NDC Package 50845-0262-2
Package Information
Vaccines (arnica montana, hypericum perforatum, ledum palustre, morbillinum, natrum muriaticum, silicea, sulphur iodatum, thuja occidentalis, urtica urens) liquids is adults & children over 12: Place 15 drops under the tongue 3 times per day.Children 2 to 12: Administer 1 drop under the tongue per year of age, 3 times per day.Children 1 and under: Administer 1 drop under the tongue, 3 times per day.For recent vaccinations, use daily for two weeks. This formulation utilizes a liquid delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0262.
Identification & Billing
Clinical Specifications
- ARNICA MONTANA WHOLE 3 [hp_X]/mL
- HYPERICUM PERFORATUM WHOLE 6 [hp_X]/mL
- MEASLES VIRUS 30 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG 30 [hp_C]/mL
- SILICON DIOXIDE 30 [hp_C]/mL
- SODIUM CHLORIDE 6 [hp_X]/mL
- SULFUR IODIDE 300 [hp_C]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 200 [hp_C]/mL
- URTICA URENS WHOLE 3 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 50845 - Liddell Laboratories, Inc.
- 50845-0262 - Vaccines
- 50845-0262-2 - 30 mL in 1 BOTTLE, DROPPER
- 50845-0262 - Vaccines
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 50845-0262-2 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Vaccines, a human over the counter drug labeled by Liddell Laboratories, Inc.. This liquid is formulated for oral use and contains arnica montana whole; hypericum perforatum whole; measles virus; rhododendron tomentosum leafy twig; silicon dioxide; sodium chloride; sulfur iodide; thuja occidentalis leafy twig; 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, Inc. on August 06, 2020. 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: 50845026202. 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.