Grief Liquid
NDC Package 43742-1513-1
Package Information
Grief (cimicifuga racemosa, natrum sulphuricum, phosphoricum acidum, sepia, cerebrum suis, ignatia amara, natrum muriaticum, ambra grisea, dna, aurum metallicum, cocculus indicus, digitalis purpurea, helleborus niger, lycopodium clavatum, staphysagria) liquids is for temporary relief of symptoms related to grief such as shock, denial, weeping, forsakenness, lack of emotion and sighing.****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 43742-1513.
Identification & Billing
Clinical Specifications
- AMBERGRIS 9 [hp_X]/mL
- ANAMIRTA COCCULUS SEED 12 [hp_X]/mL
- BLACK COHOSH 6 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 12 [hp_X]/mL
- DIGITALIS 12 [hp_X]/mL
- GOLD 12 [hp_X]/mL
- HELLEBORUS NIGER ROOT 12 [hp_X]/mL
- HERRING SPERM DNA 10 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- PHOSPHORIC ACID 6 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 8 [hp_X]/mL
- SODIUM CHLORIDE 8 [hp_X]/mL
- SODIUM SULFATE 6 [hp_X]/mL
- STRYCHNOS IGNATII SEED 8 [hp_X]/mL
- SUS SCROFA CEREBRUM 8 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-1513 - Grief
- 43742-1513-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-1513 - Grief
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 43742-1513-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Grief, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains ambergris; anamirta cocculus seed; black cohosh; delphinium staphisagria seed; digitalis; gold; helleborus niger root; herring sperm dna; lycopodium clavatum spore; phosphoric acid; sepia officinalis juice; sodium chloride; sodium sulfate; strychnos ignatii seed; sus scrofa cerebrum 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 26, 2019. 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: 43742151301. 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.