Home NDC 87267-001 EAYONYUM STYE RELIEF SERUM
Product NDC 87267-001
11-digit product format 872670001
Labeler code 87267
Product ID 87267-001_456d9c2e-91d3-b971-e063-6394a90adee7
Type HUMAN OTC DRUG
Nonproprietary name Gentiana Scabra Root Extract
Dosage form LIQUID
Route OPHTHALMIC
Labeler YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-08
Substance GENTIANA SCABRA ROOT
Active strength .6 g/100mL
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 EAYONYUM STYE RELIEF SERUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GENTIANA SCABRA ROOT .6 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination GXZ33VNT92 Internal UNII lookup
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 87267-001-01 EAYONYUM STYE RELIEF SERUM 30 mL in 1 BOTTLE LIQUID 30 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 87267-001-01 87267000101 30 mL in 1 BOTTLE (87267-001-01) 30 ml 2025-12-08 No No Current