57955-9966 NDC - CONSTITUTIONAL ENHANCER (ACONITUM NAPELLUS, ARSENICUM ALBUM, BARYTA CARBONICA, BRYONIA, CALCAREA CARBONICA, CANTHARIS, GELSEMIUM SEMPERVIRENS, GRAPHITES, HYDRASTIS CANADENSIS, KALI IODATUM, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, NATRUM MURIATICUM, NUX VOMICA, PHOSPHORUS, PHYTOLACCA DECANDRA, PULSATILLA, RHUS TOX, SEPIA, SILICEA AND SULPHUR.)

Drug Information

  • Product NDC: 57955-9966
  • Proprietary Name: Constitutional Enhancer
  • Non Proprietary Name: Aconitum napellus, Arsenicum album, Baryta carbonica, Bryonia, Calcarea carbonica, Cantharis, Gelsemium sempervirens, Graphites, Hydrastis canadensis, Kali iodatum, Lachesis mutus, Lycopodium clavatum, Mercurius vivus, Natrum muriaticum, Nux vomica, Phosphorus, Phytolacca decandra, Pulsatilla, Rhus tox, Sepia, Silicea and Sulphur.
  • Active Ingredient(s): 10 [hp_X]/59mL ACONITUM NAPELLUS WHOLE; 10 [hp_X]/59mL ARSENIC TRIOXIDE; 10 [hp_X]/59mL BARIUM CARBONATE; 10 [hp_X]/59mL BRYONIA ALBA ROOT; 10 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT; 10 [hp_X]/59mL GOLDENSEAL; 10 [hp_X]/59mL GRAPHITE; 10 [hp_X]/59mL LACHESIS MUTA VENOM; 10 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE; 10 [hp_X]/59mL LYTTA VESICATORIA; 10 [hp_X]/59mL MERCURY; 10 [hp_X]/59mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 10 [hp_X]/59mL PHOSPHORUS; 10 [hp_X]/59mL PHYTOLACCA AMERICANA ROOT; 10 [hp_X]/59mL POTASSIUM IODIDE; 10 [hp_X]/59mL PULSATILLA VULGARIS WHOLE; 10 [hp_X]/59mL SEPIA OFFICINALIS JUICE; 10 [hp_X]/59mL SILICON DIOXIDE; 10 [hp_X]/59mL SODIUM CHLORIDE; 10 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED; 10 [hp_X]/59mL SULFUR; 10 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [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:3/13/2026

Package Information

No. Package Code Package Description Billing Unit
157955-9966-259 mL in 1 BOTTLE, SPRAY (57955-9966-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57955-9966The 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 NAMEConstitutional EnhancerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAconitum napellus, Arsenicum album, Baryta carbonica, Bryonia, Calcarea carbonica, Cantharis, Gelsemium sempervirens, Graphites, Hydrastis canadensis, Kali iodatum, Lachesis mutus, Lycopodium clavatum, Mercurius vivus, Natrum muriaticum, Nux vomica, Phosphorus, Phytolacca decandra, Pulsatilla, Rhus tox, Sepia, Silicea 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 DATE3/13/2026This 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 NAMEACONITUM NAPELLUS WHOLE; ARSENIC TRIOXIDE; BARIUM CARBONATE; BRYONIA ALBA ROOT; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; GRAPHITE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; LYTTA VESICATORIA; MERCURY; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM IODIDE; PULSATILLA VULGARIS WHOLE; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; SULFUR; TOXICODENDRON PUBESCENS LEAFAn 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; 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; [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], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS] 

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

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