62106-0601 NDC - FUNGISODE (ARSENICUM ALBUM, BERBERIS VULGARIS, CALCAREA CARBONICA, CANDIDA ALBICANS, CARBO VEGETABILIS, CHELIDONIUM MAJUS, ECHINACEA PURPUREA, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, MURIATICUM ACIDUM, NITRICUM ACIDUM, OXALICUM ACIDUM, SEPIA OFFICINALIS, SULPHUR)

Drug Information

Product NDC: 62106-0601

Proprietary Name: Fungisode

Non Proprietary Name: Arsenicum album, Berberis vulgaris, Calcarea carbonica, Candida albicans, Carbo vegetabilis, Chelidonium majus, Echinacea purpurea, Hepar sulphuris calcareum, Kreosotum, Lycopodium clavatum, Mercurius solubilis, Muriaticum acidum, Nitricum acidum, Oxalicum acidum, Sepia officinalis, Sulphur

Active Ingredient(s):
  • 7 [hp_C]/30mL ACTIVATED CHARCOAL;
  • 4 [hp_C]/30mL ARSENIC TRIOXIDE;
  • 4 [hp_C]/30mL BERBERIS VULGARIS ROOT BARK;
  • 5 [hp_C]/30mL CALCIUM SULFIDE;
  • 12 [hp_X]/30mL CANDIDA ALBICANS;
  • 4 [hp_C]/30mL CHELIDONIUM MAJUS ROOT;
  • 3 [hp_X]/30mL ECHINACEA PURPUREA FLOWERING TOP;
  • 7 [hp_C]/30mL HYDROCHLORIC ACID;
  • 5 [hp_C]/30mL LYCOPODIUM CLAVATUM SPORE;
  • 5 [hp_C]/30mL MERCURIUS SOLUBILIS;
  • 5 [hp_C]/30mL NITRIC ACID;
  • 8 [hp_X]/30mL OXALIC ACID DIHYDRATE;
  • 8 [hp_X]/30mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 5 [hp_C]/30mL SEPIA OFFICINALIS JUICE;
  • 4 [hp_C]/30mL SULFUR;
  • 5 [hp_C]/30mL WOOD CREOSOTE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Fungal Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Non-Standardized Fungal Allergenic Extract [EPC]

Labeler Information

Labeler Name: Seroyal USA
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/2/2017

Package Information

No. Package Code Package Description Billing Unit
162106-0601-01 BOTTLE, GLASS in 1 CARTON (62106-0601-0) / 30 mL in 1 BOTTLE, GLASS

NDC Record

Field Name Field Value Definition
PRODUCT NDC62106-0601The 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 NAMEFungisodeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEArsenicum album, Berberis vulgaris, Calcarea carbonica, Candida albicans, Carbo vegetabilis, Chelidonium majus, Echinacea purpurea, Hepar sulphuris calcareum, Kreosotum, Lycopodium clavatum, Mercurius solubilis, Muriaticum acidum, Nitricum acidum, Oxalicum acidum, Sepia officinalis, SulphurThe 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 DATE8/2/2017This 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 NAMESeroyal USAName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACTIVATED CHARCOAL; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; CALCIUM SULFIDE; CANDIDA ALBICANS; CHELIDONIUM MAJUS ROOT; ECHINACEA PURPUREA FLOWERING TOP; HYDROCHLORIC ACID; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; NITRIC ACID; OXALIC ACID DIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEPIA OFFICINALIS JUICE; SULFUR; WOOD CREOSOTEAn 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 STRENGTH7; 4; 4; 5; 12; 4; 3; 7; 5; 5; 5; 8; 8; 5; 4; 5 
ACTIVE INGRED UNIT[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC] 

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This page was last updated on: 2/1/2023