57955-9974 NDC - HEADACHE AND MIGRAINE RELIEF (BELLADONNA, BRYONIA, CAPSICUM ANNUUM, GELSEMIUM, GLONOINUM, IGNATIA AMARA, KALI BICHROMICUM, KALI CARBONICUM, LYCOPODIUM, NATRUM MURIATICUM, NICCOLUM METALLICUM, NUX VOMICA, SANGUINARIA, SECALE CORNUTUM, SPIGELIA ANTH AND SULPHUR.)

Drug Information

  • Product NDC: 57955-9974
  • Proprietary Name: Headache and Migraine Relief
  • Non Proprietary Name: Belladonna, Bryonia, Capsicum annuum, Gelsemium, Glonoinum, Ignatia amara, Kali bichromicum, Kali carbonicum, Lycopodium, Natrum muriaticum, Niccolum metallicum, Nux vomica, Sanguinaria, Secale cornutum, Spigelia anth and Sulphur.
  • Active Ingredient(s): 10 [hp_X]/59mL ATROPA BELLADONNA; 10 [hp_X]/59mL BRYONIA ALBA ROOT; 10 [hp_X]/59mL CAPSICUM; 10 [hp_X]/59mL CLAVICEPS PURPUREA SCLEROTIUM; 10 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT; 10 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE; 10 [hp_X]/59mL NICKEL; 10 [hp_X]/59mL NITROGLYCERIN; 10 [hp_X]/59mL POTASSIUM CARBONATE; 10 [hp_X]/59mL POTASSIUM DICHROMATE; 10 [hp_X]/59mL SANGUINARIA CANADENSIS ROOT; 10 [hp_X]/59mL SODIUM CHLORIDE; 10 [hp_X]/59mL SPIGELIA ANTHELMIA WHOLE; 10 [hp_X]/59mL STRYCHNOS IGNATII SEED; 10 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED; 10 [hp_X]/59mL SULFUR
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Nitrate Vasodilator [EPC]; Nitrates [CS]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Standardized Chemical Allergen [EPC]; Vasodilation [PE]; Vegetable 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:3/10/2026

Package Information

No. Package Code Package Description Billing Unit
157955-9974-259 mL in 1 BOTTLE, SPRAY (57955-9974-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-9974The 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 NAMEHeadache and Migraine ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBelladonna, Bryonia, Capsicum annuum, Gelsemium, Glonoinum, Ignatia amara, Kali bichromicum, Kali carbonicum, Lycopodium, Natrum muriaticum, Niccolum metallicum, Nux vomica, Sanguinaria, Secale cornutum, Spigelia anth and Sulphur.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 DATE3/10/2026This 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 NAMEATROPA BELLADONNA; BRYONIA ALBA ROOT; CAPSICUM; CLAVICEPS PURPUREA SCLEROTIUM; GELSEMIUM SEMPERVIRENS ROOT; LYCOPODIUM CLAVATUM SPORE; NICKEL; NITROGLYCERIN; POTASSIUM CARBONATE; POTASSIUM DICHROMATE; SANGUINARIA CANADENSIS ROOT; SODIUM CHLORIDE; SPIGELIA ANTHELMIA WHOLE; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; SULFURAn 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], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Chemical Allergen [EPC], Vasodilation [PE], Vegetable Proteins [CS] 

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This page was last updated on: 4/14/2026

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