62106-0625 NDC - HKI (ATROPINUM SULPHURICUM, BENZOICUM ACIDUM, BERBERIS VULGARIS, CALCAREA CARBONICA, COLOCYNTHIS, COCCUS CACTI, LAPIS ALBUS, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, ORYCTOLAGUS CUNICULUS KIDNEY, RUBIA TINCTORUM, SARSAPARILLA, URTICA URENS)

Drug Information

  • Product NDC: 62106-0625
  • Proprietary Name: HKI
  • Non Proprietary Name: Atropinum sulphuricum, Benzoicum acidum, Berberis vulgaris, Calcarea carbonica, Colocynthis, Coccus cacti, Lapis albus, Lithium carbonicum, Lycopodium clavatum, Oryctolagus cuniculus kidney, Rubia tinctorum, Sarsaparilla, Urtica urens
  • Active Ingredient(s): 6 [hp_X]/30mL ATROPINE SULFATE; 6 [hp_X]/30mL BENZOIC ACID; 5 [hp_X]/30mL BERBERIS VULGARIS ROOT BARK; 12 [hp_C]/30mL CALCIUM HEXAFLUOROSILICATE; 6 [hp_X]/30mL CITRULLUS COLOCYNTHIS FRUIT PULP; 6 [hp_X]/30mL LITHIUM CARBONATE; 5 [hp_X]/30mL LYCOPODIUM CLAVATUM SPORE; 10 [hp_X]/30mL ORYCTOLAGUS CUNICULUS KIDNEY; 12 [hp_X]/30mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 5 [hp_X]/30mL PROTORTONIA CACTI; 4 [hp_X]/30mL RUBIA TINCTORUM ROOT; 1 [hp_X]/30mL SARSAPARILLA; 1 [hp_X]/30mL URTICA URENS
  • Administration Route(s): SUBLINGUAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Ammonium Ion Binding Activity [MoA]; Anticholinergic [EPC]; Cholinergic Antagonists [MoA]; Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]; Mood Stabilizer [EPC]; Nitrogen Binding Agent [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Seroyal USA
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/14/2015

Package Information

No. Package Code Package Description Billing Unit
162106-0625-01 BOTTLE, GLASS in 1 CARTON (62106-0625-0) / 30 mL in 1 BOTTLE, GLASS

NDC Record

Field Name Field Value Definition
PRODUCT NDC62106-0625The 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 NAMEHKIThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAtropinum sulphuricum, Benzoicum acidum, Berberis vulgaris, Calcarea carbonica, Colocynthis, Coccus cacti, Lapis albus, Lithium carbonicum, Lycopodium clavatum, Oryctolagus cuniculus kidney, Rubia tinctorum, Sarsaparilla, Urtica urensThe 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 NAMESUBLINGUALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/14/2015This 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 NAMEATROPINE SULFATE; BENZOIC ACID; BERBERIS VULGARIS ROOT BARK; CALCIUM HEXAFLUOROSILICATE; CITRULLUS COLOCYNTHIS FRUIT PULP; LITHIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; ORYCTOLAGUS CUNICULUS KIDNEY; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PROTORTONIA CACTI; RUBIA TINCTORUM ROOT; SARSAPARILLA; URTICA URENSAn 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; 6; 5; 12; 6; 6; 5; 10; 12; 5; 4; 1; 1 
ACTIVE INGRED UNIT[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL 
PHARM CLASSESAmmonium Ion Binding Activity [MoA], Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], Mood Stabilizer [EPC], Nitrogen Binding Agent [EPC] 

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This page was last updated on: 2/5/2026

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