Sinu Hc Liquid
NDC Package 43742-1985-1
Package Information
Sinu Hc (plantago major, pulsatilla (pratensis), luffa operculata, mercurius iodatus ruber, mucosa nasalis suis, euphorbium officinarum, argentum nitricum, hepar sulphuris calcareum, calcarea carbonica, natrum muriaticum, sinusitisinum) liquids is for temporary relief of symptoms of acute and chronic sinusitis.****These statements are based upon homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-1985.
Identification & Billing
Clinical Specifications
- CALCIUM SULFIDE 10 [hp_X]/mL
- EUPHORBIA RESINIFERA RESIN 9 [hp_X]/mL
- LUFFA OPERCULATA FRUIT 6 [hp_X]/mL
- MERCURIC IODIDE 8 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- PLANTAGO MAJOR WHOLE 3 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 4 [hp_X]/mL
- SILVER NITRATE 10 [hp_X]/mL
- SINUSITISINUM 20 [hp_X]/mL
- SODIUM CHLORIDE 12 [hp_X]/mL
- SUS SCROFA NASAL MUCOSA 8 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-1985 - Sinu Hc
- 43742-1985-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-1985 - Sinu Hc
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 43742-1985-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Sinu Hc, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains calcium sulfide; euphorbia resinifera resin; luffa operculata fruit; mercuric iodide; oyster shell calcium carbonate, crude; plantago major whole; pulsatilla pratensis whole; silver nitrate; sinusitisinum; sodium chloride; sus scrofa nasal mucosa 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 March 26, 2021. 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: 43742198501. 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.