62185-0064 NDC - BREAD CRAVINGS (ACETALDEHYDE, COUMARINUM, HISTAMINUM HYDROCHLORICUM, QUERCETIN, TORULA CEREVISIAE, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, ADRENOCORTICOTROPHIN, SARCOLACTICUM ACIDUM, SEPIA, ADRENOCORTICOTROPHIN, FAECALIS (ALKALIGENES))

Drug Information

  • Product NDC: 62185-0064
  • Proprietary Name: Bread Cravings
  • Non Proprietary Name: Acetaldehyde, Coumarinum, Histaminum Hydrochloricum, Quercetin, Torula Cerevisiae, Candida Albicans, Candida Parapsilosis, Adrenocorticotrophin, Sarcolacticum Acidum, Sepia, Adrenocorticotrophin, Faecalis (Alkaligenes)
  • Active Ingredient(s): 6 [hp_X]/mL ACETALDEHYDE; 30 [hp_C]/mL ALCALIGENES FAECALIS; 12 [hp_X]/mL CANDIDA ALBICANS; 12 [hp_X]/mL CANDIDA PARAPSILOSIS; 15 [hp_C]/mL CORTICOTROPIN HUMAN; 6 [hp_X]/mL COUMARIN; 6 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE; 6 [hp_C]/mL LACTIC ACID, L-; 6 [hp_X]/mL QUERCETIN; 10 [hp_X]/mL SACCHAROMYCES CEREVISIAE; 6 [hp_C]/mL SEPIA OFFICINALIS JUICE
  • 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]; Fungal Proteins [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Dr. Donna Restivo DC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/21/2021

Package Information

No. Package Code Package Description Billing Unit
162185-0064-130 mL in 1 BOTTLE, DROPPER (62185-0064-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62185-0064The 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 NAMEBread CravingsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAcetaldehyde, Coumarinum, Histaminum Hydrochloricum, Quercetin, Torula Cerevisiae, Candida Albicans, Candida Parapsilosis, Adrenocorticotrophin, Sarcolacticum Acidum, Sepia, Adrenocorticotrophin, Faecalis (Alkaligenes)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 DATE6/21/2021This 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 NAMEDr. Donna Restivo DCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACETALDEHYDE; ALCALIGENES FAECALIS; CANDIDA ALBICANS; CANDIDA PARAPSILOSIS; CORTICOTROPIN HUMAN; COUMARIN; HISTAMINE DIHYDROCHLORIDE; LACTIC ACID, L-; QUERCETIN; SACCHAROMYCES CEREVISIAE; SEPIA OFFICINALIS JUICEAn 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 STRENGTH6; 30; 12; 12; 15; 6; 6; 6; 6; 10; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC] 

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This page was last updated on: 11/21/2025

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