Sore Throat And Laryngitis Liquid
NDC Package 57955-9967-2
Package Information
Sore Throat And Laryngitis (aconitum napellus, antimonium crudum, arum triphyllum, borax, causticum, ferrum phos, graphites, hepar sulph calc, kali bichromicum, phosphorus, selenium metallicum and spongia tosta.) liquids is uses † For temporary relief of minor sore throat symptoms:drynessburningticklinghoarsenessrough voice from overuselaryngitis (loss of voice) † Claims based on traditional Homeopathic practice, not accepted medical evidence, notFDA evaluated. This formulation utilizes a liquid delivery system. Marketed by King Bio Inc., this product is identified by NDC 57955-9967.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS WHOLE 10 [hp_X]/59mL
- ANTIMONY TRISULFIDE 10 [hp_X]/59mL
- ARISAEMA TRIPHYLLUM ROOT 10 [hp_X]/59mL
- CALCIUM SULFIDE 10 [hp_X]/59mL
- CAUSTICUM 10 [hp_X]/59mL
- FERROSOFERRIC PHOSPHATE 10 [hp_X]/59mL
- GRAPHITE 10 [hp_X]/59mL
- PHOSPHORUS 10 [hp_X]/59mL
- POTASSIUM DICHROMATE 10 [hp_X]/59mL
- SELENIUM 10 [hp_X]/59mL
- SODIUM BORATE 10 [hp_X]/59mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 10 [hp_X]/59mL
Regulatory & Marketing
Hierarchy Structure
- 57955 - King Bio Inc.
- 57955-9967 - Sore Throat And Laryngitis
- 57955-9967-2 - 59 mL in 1 BOTTLE, SPRAY
- 57955-9967 - Sore Throat And Laryngitis
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 57955-9967-2 identifies a specific commercial package of 59 ml in 1 bottle, spray of Sore Throat And Laryngitis, a human over the counter drug labeled by King Bio Inc.. This liquid is formulated for oral use and contains aconitum napellus whole; antimony trisulfide; arisaema triphyllum root; calcium sulfide; causticum; ferrosoferric phosphate; graphite; phosphorus; potassium dichromate; selenium; sodium borate; spongia officinalis skeleton, roasted 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 King Bio Inc. on March 13, 2026. The current certification is valid through December 31, 2027.
How is this King Bio Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 57955996702. 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.