Home NDC 17312-478 Natural Eyes Floaters Relief
Product NDC 17312-478
11-digit product format 173120478
Labeler code 17312
Product ID 17312-478_445dc839-50b1-efd8-e063-6394a90ac00b
Type HUMAN OTC DRUG
Nonproprietary name Chelidonium, Euphrasia, Kali sulph, Natrum muriaticum, Phosphorus, Physostigma, Sepia, Silicea
Dosage form TABLET
Route ORAL
Labeler TRP Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-04-28
Substance SODIUM CHLORIDE; POTASSIUM SULFATE; EUPHRASIA STRICTA; PHYSOSTIGMA VENENOSUM SEED; SILICON DIOXIDE; SEPIA OFFICINALIS JUICE; CHELIDONIUM MAJUS; PHOSPHORUS
Active strength 10; 10; 6; 12; 12; 7; 6; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Natural Eyes Floaters Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 10 [hp_X]/1 POTASSIUM SULFATE 10 [hp_X]/1 EUPHRASIA STRICTA 6 [hp_X]/1 PHYSOSTIGMA VENENOSUM SEED 12 [hp_X]/1 SILICON DIOXIDE 12 [hp_X]/1 SEPIA OFFICINALIS JUICE 7 [hp_X]/1 CHELIDONIUM MAJUS 6 [hp_X]/1 PHOSPHORUS 12 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17312-478-14 Natural Eyes Floaters Relief 1 in 1 PACKAGE TABLET 1 1 17312-478-14 Natural Eyes Floaters Relief 70 in 1 BOTTLE TABLET 70 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 17312-478-14 17312047814 1 BOTTLE in 1 PACKAGE (17312-478-14) / 70 TABLET in 1 BOTTLE 1 bottle 2025-04-28 No No Current