57955-9983 NDC - SNORE CONTROL (BROMIUM, CHAMOMILLA, CINCHONA, CUPRUM METALLICUM, HELLEBORUS NIGER, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, LAUROCERASUS, NUX VOMICA, PHOSPHORICUM ACIDUM, RHUS TOX, SILICEA, STRAMONIUM, SULPHUR AND ZINCUM METALLICUM.)

Drug Information

  • Product NDC: 57955-9983
  • Proprietary Name: Snore Control
  • Non Proprietary Name: Bromium, Chamomilla, Cinchona, Cuprum metallicum, Helleborus niger, Histaminum hydrochloricum, Hydrastis canadensis, Kali bichromicum, Laurocerasus, Nux vomica, Phosphoricum acidum, Rhus tox, Silicea, Stramonium, Sulphur and Zincum metallicum.
  • Active Ingredient(s): 10 [hp_X]/59mL BROMINE; 10 [hp_X]/59mL CINCHONA OFFICINALIS BARK; 10 [hp_X]/59mL COPPER; 10 [hp_X]/59mL DATURA STRAMONIUM; 10 [hp_X]/59mL GOLDENSEAL; 10 [hp_X]/59mL HELLEBORUS NIGER ROOT; 10 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE; 10 [hp_X]/59mL MATRICARIA CHAMOMILLA WHOLE; 10 [hp_X]/59mL PHOSPHORIC ACID; 10 [hp_X]/59mL POTASSIUM DICHROMATE; 10 [hp_X]/59mL PRUNUS LAUROCERASUS LEAF; 10 [hp_X]/59mL SILICON DIOXIDE; 10 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED; 10 [hp_X]/59mL SULFUR; 10 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF; 10 [hp_X]/59mL ZINC
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Inhibit Ovum Fertilization [PE]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: King Bio Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/15/2026

Package Information

No. Package Code Package Description Billing Unit
157955-9983-259 mL in 1 BOTTLE, SPRAY (57955-9983-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-9983The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMESnore ControlThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBromium, Chamomilla, Cinchona, Cuprum metallicum, Helleborus niger, Histaminum hydrochloricum, Hydrastis canadensis, Kali bichromicum, Laurocerasus, Nux vomica, Phosphoricum acidum, Rhus tox, Silicea, Stramonium, Sulphur and Zincum metallicum.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/15/2026This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEKing Bio Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBROMINE; CINCHONA OFFICINALIS BARK; COPPER; DATURA STRAMONIUM; GOLDENSEAL; HELLEBORUS NIGER ROOT; HISTAMINE DIHYDROCHLORIDE; MATRICARIA CHAMOMILLA WHOLE; PHOSPHORIC ACID; POTASSIUM DICHROMATE; PRUNUS LAUROCERASUS LEAF; SILICON DIOXIDE; STRYCHNOS NUX-VOMICA SEED; SULFUR; TOXICODENDRON PUBESCENS LEAF; ZINCAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS] 

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This page was last updated on: 3/27/2026

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