17312-172 NDC - EYE STRAIN RELIEF (ACONITUM NAPELLUS - APIS MELLIFERA - SILVER NITRATE - EUPHRASIA STRICTA - SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE -)

Drug Information

Product NDC: 17312-172

Proprietary Name: Eye Strain Relief

Non Proprietary Name: ACONITUM NAPELLUS - APIS MELLIFERA - SILVER NITRATE - EUPHRASIA STRICTA - SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE -

Active Ingredient(s):
  • 6 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP;
  • 6 [hp_X]/mL EUPHRASIA STRICTA;
  • 13 [hp_X]/mL PHYSOSTIGMA VENENOSUM SEED;
  • 6 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP;
  • 8 [hp_X]/mL SODIUM CHLORIDE;
  • 6 [hp_X]/mL POLYGALA SENEGA ROOT


Administration Route(s): OPHTHALMIC

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: TRP Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/27/2018

Package Information

No. Package Code Package Description Billing Unit
117312-172-151 BOTTLE, DROPPER in 1 PACKAGE (17312-172-15) > 10 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17312-172The 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 Strain 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 NAMEACONITUM NAPELLUS - APIS MELLIFERA - SILVER NITRATE - EUPHRASIA STRICTA - SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE -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 NAMEOPHTHALMICThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/27/2018This 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 NAMERUTA GRAVEOLENS FLOWERING TOP; EUPHRASIA STRICTA; PHYSOSTIGMA VENENOSUM SEED; CONIUM MACULATUM FLOWERING TOP; SODIUM CHLORIDE; POLYGALA SENEGA ROOTThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH6; 6; 13; 6; 8; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 

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This page was last updated on: 2/19/2021