62106-1120 NDC - UNDA 21 (CONDURANGO, CALENDULA OFFICINALIS, CAMPHORA, HYDRASTIS CANADENSIS, THUJA OCCIDENTALIS, ALUMINIUM METALLICUM, AURUM METALLICUM)

Drug Information

Product NDC: 62106-1120

Proprietary Name: UNDA 21

Non Proprietary Name: Condurango, Calendula officinalis, Camphora, Hydrastis canadensis, Thuja occidentalis, Aluminium metallicum, Aurum metallicum

Active Ingredient(s):
  • 12 [hp_X]/20mL ALUMINUM;
  • 4 [hp_X]/20mL CALENDULA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/20mL CAMPHOR (NATURAL);
  • 12 [hp_X]/20mL GOLD;
  • 4 [hp_X]/20mL GOLDENSEAL;
  • 4 [hp_X]/20mL MARSDENIA CONDURANGO BARK;
  • 4 [hp_X]/20mL THUJA OCCIDENTALIS LEAFY TWIG


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Standardized Chemical Allergen [EPC]

Labeler Information

Labeler Name: Seroyal USA
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/26/2015

Package Information

No. Package Code Package Description Billing Unit
162106-1120-81 BOTTLE, GLASS in 1 CARTON (62106-1120-8) / 20 mL in 1 BOTTLE, GLASS

NDC Record

Field Name Field Value Definition
PRODUCT NDC62106-1120The 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 NAMEUNDA 21The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECondurango, Calendula officinalis, Camphora, Hydrastis canadensis, Thuja occidentalis, Aluminium metallicum, Aurum metallicumThe 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 DATE5/26/2015This 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 NAMEALUMINUM; CALENDULA OFFICINALIS FLOWERING TOP; CAMPHOR (NATURAL); GOLD; GOLDENSEAL; MARSDENIA CONDURANGO BARK; THUJA OCCIDENTALIS LEAFY TWIGAn 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 STRENGTH12; 4; 4; 12; 4; 4; 4 
ACTIVE INGRED UNIT[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] 

Download Record

Download this NDC record in Text format: Export

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

Download this NDC record in XML format: Export

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