Spectric Liquid
NDC Package 43742-2191-1
Package Information
Spectric (agaricus muscarius, aspartame, bufo rana, carcinosin, cerebrum suis, ethylicum, helleborus niger, hydrogen, hyoscyamus niger, kali bromatum, l-dopa, neon, olibanum (boswellia serrata), placenta totalis suis, serotonin (hydrochloride), stramonium, thuja occidentalis) liquids is 1-10 drops under the tongue, 3 times a day or as directed by a health professional. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc, this product is identified by NDC 43742-2191.
Identification & Billing
Clinical Specifications
- ALCOHOL 6 [hp_X]/mL
- AMANITA MUSCARIA FRUITING BODY 12 [hp_X]/mL
- ASPARTAME 6 [hp_X]/mL
- BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/mL
- DATURA STRAMONIUM 12 [hp_X]/mL
- HELLEBORUS NIGER ROOT 12 [hp_X]/mL
- HUMAN BREAST TUMOR CELL 30 [hp_X]/mL
- HYDROGEN 12 [hp_C]/mL
- HYOSCYAMUS NIGER 12 [hp_X]/mL
- INDIAN FRANKINCENSE 12 [hp_X]/mL
- LEVODOPA 6 [hp_X]/mL
- NEON 16 [hp_C]/mL
- POTASSIUM BROMIDE 6 [hp_X]/mL
- SEROTONIN HYDROCHLORIDE 6 [hp_X]/mL
- SUS SCROFA CEREBRUM 8 [hp_X]/mL
- SUS SCROFA PLACENTA 8 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc
- 43742-2191 - Spectric
- 43742-2191-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-2191 - Spectric
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 43742-2191-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Spectric, a human over the counter drug labeled by Deseret Biologicals, Inc. This liquid is formulated for oral use and contains alcohol; amanita muscaria fruiting body; aspartame; bufo bufo cutaneous gland; datura stramonium; helleborus niger root; human breast tumor cell; hydrogen; hyoscyamus niger; indian frankincense; levodopa; neon; potassium bromide; serotonin hydrochloride; sus scrofa cerebrum; sus scrofa placenta; thuja occidentalis leafy twig 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 September 23, 2024. 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: 43742219101. 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.