57955-9968 NDC - SKIN IRRITATIONS AND ITCH RELIEF (AGARICUS MUSCARIUS, ALUMINA, ANAGALLIS ARVENSIS, ANTIMONIUM TARTARICUM, APIS MELLIFICA, ARSENICUM ALBUM, ARSENICUM IODATUM, BOVISTA, CAUSTICUM, DOLICHOS PRURIENS, FAGOPYRUM ESCULENTUM, GRAPHITES, KALI MURIATICUM, MURIATICUM ACIDUM, OLEANDER, PETROLEUM, PIX LIQUIDA, RADIUM BROMATUM (12X, 30X, 1LM), RHUS TOX, SELENIUM METALLICUM, SULPHUR AND URTICA URENS.)

Drug Information

  • Product NDC: 57955-9968
  • Proprietary Name: Skin Irritations and Itch Relief
  • Non Proprietary Name: Agaricus muscarius, Alumina, Anagallis arvensis, Antimonium tartaricum, Apis mellifica, Arsenicum album, Arsenicum iodatum, Bovista, Causticum, Dolichos pruriens, Fagopyrum esculentum, Graphites, Kali muriaticum, Muriaticum acidum, Oleander, Petroleum, Pix liquida, Radium bromatum (12X, 30X, 1LM), Rhus tox, Selenium metallicum, Sulphur and Urtica urens.
  • Active Ingredient(s): 10 [hp_X]/59mL ALUMINUM OXIDE; 10 [hp_X]/59mL AMANITA MUSCARIA FRUITING BODY; 10 [hp_X]/59mL ANTIMONY POTASSIUM TARTRATE; 10 [hp_X]/59mL APIS MELLIFERA; 10 [hp_X]/59mL ARSENIC TRIIODIDE; 10 [hp_X]/59mL ARSENIC TRIOXIDE; 10 [hp_X]/59mL CAUSTICUM; 10 [hp_X]/59mL FAGOPYRUM ESCULENTUM WHOLE; 10 [hp_X]/59mL GRAPHITE; 10 [hp_X]/59mL HYDROCHLORIC ACID; 10 [hp_X]/59mL LIQUID PETROLEUM; 10 [hp_X]/59mL LYCOPERDON UTRIFORME FRUITING BODY; 10 [hp_X]/59mL LYSIMACHIA ARVENSIS WHOLE; 10 [hp_X]/59mL MUCUNA PRURIENS FRUIT TRICHOME; 10 [hp_X]/59mL NERIUM OLEANDER LEAF; 10 [hp_X]/59mL PINE TAR; 10 [hp_X]/59mL POTASSIUM CHLORIDE; 12 [hp_X]/59mL RADIUM BROMIDE; 10 [hp_X]/59mL SELENIUM; 10 [hp_X]/59mL SULFUR; 10 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF; 10 [hp_X]/59mL URTICA URENS WHOLE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Salt [EPC]; Standardized Insect Venom Allergenic Extract [EPC]

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:3/13/2026

Package Information

No. Package Code Package Description Billing Unit
157955-9968-259 mL in 1 BOTTLE, SPRAY (57955-9968-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-9968The 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 NAMESkin Irritations and Itch ReliefThis is the date that the labeler indicates was the start of its marketing of the drug product.
NON PROPRIETARY NAMEAgaricus muscarius, Alumina, Anagallis arvensis, Antimonium tartaricum, Apis mellifica, Arsenicum album, Arsenicum iodatum, Bovista, Causticum, Dolichos pruriens, Fagopyrum esculentum, Graphites, Kali muriaticum, Muriaticum acidum, Oleander, Petroleum, Pix liquida, Radium bromatum (12X, 30X, 1LM), Rhus tox, Selenium metallicum, Sulphur and Urtica urens.This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/13/2026This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEKing Bio Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALUMINUM OXIDE; AMANITA MUSCARIA FRUITING BODY; ANTIMONY POTASSIUM TARTRATE; APIS MELLIFERA; ARSENIC TRIIODIDE; ARSENIC TRIOXIDE; CAUSTICUM; FAGOPYRUM ESCULENTUM WHOLE; GRAPHITE; HYDROCHLORIC ACID; LIQUID PETROLEUM; LYCOPERDON UTRIFORME FRUITING BODY; LYSIMACHIA ARVENSIS WHOLE; MUCUNA PRURIENS FRUIT TRICHOME; NERIUM OLEANDER LEAF; PINE TAR; POTASSIUM CHLORIDE; RADIUM BROMIDE; SELENIUM; SULFUR; TOXICODENDRON PUBESCENS LEAF; URTICA URENS WHOLEAn 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; 10; 12; 10; 10; 10; 10Product 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.
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; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 
PHARM CLASSESAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Insect Venom Allergenic Extract [EPC] 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

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

Previous Code
Next Code