17312-040 NDC - EYE TWITCHING RELIEF (AMANITA MUSCARIA FRUITING BODY, COPPER, EUPHRASIA STRICTA, PILOCARPUS JABORANDII WHOLE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHYSOSTIGMA VENENOSUM SEED, TIN)

Drug Information

Product NDC: 17312-040

Proprietary Name: Eye Twitching Relief

Non Proprietary Name: AMANITA MUSCARIA FRUITING BODY, COPPER, EUPHRASIA STRICTA, PILOCARPUS JABORANDII WHOLE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHYSOSTIGMA VENENOSUM SEED, TIN

Active Ingredient(s):
  • 7 [hp_X]/mL AMANITA MUSCARIA FRUITING BODY;
  • 12 [hp_X]/mL COPPER;
  • 6 [hp_X]/mL EUPHRASIA STRICTA;
  • 11 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE;
  • 6 [hp_X]/mL PHYSOSTIGMA VENENOSUM SEED;
  • 9 [hp_X]/mL PILOCARPUS JABORANDII WHOLE;
  • 12 [hp_X]/mL TIN


Administration Route(s): OPHTHALMIC

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Calculi Dissolution Agent [EPC];
  • Copper [CS];
  • Copper-containing Intrauterine Device [EPC];
  • Decreased Embryonic Implantation [PE];
  • Decreased Sperm Motility [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibit Ovum Fertilization [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Labeler Name: TRP Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/1/2018

Package Information

No. Package Code Package Description Billing Unit
117312-040-151 BOTTLE, DROPPER in 1 PACKAGE (17312-040-15) / 10 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17312-040The 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 NAMEEye Twitching ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAMANITA MUSCARIA FRUITING BODY, COPPER, EUPHRASIA STRICTA, PILOCARPUS JABORANDII WHOLE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHYSOSTIGMA VENENOSUM SEED, TINThe 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 NAMEOPHTHALMICThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/1/2018This 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 NAMETRP CompanyName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMANITA MUSCARIA FRUITING BODY; COPPER; EUPHRASIA STRICTA; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PHYSOSTIGMA VENENOSUM SEED; PILOCARPUS JABORANDII WHOLE; TINAn 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; 12; 6; 11; 6; 9; 12 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESCalculi Dissolution Agent [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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