Home NDC 84896-005 STYE EYE RELIEF SERUM
Product NDC 84896-005
11-digit product format 848960005
Labeler code 84896
Product ID 84896-005_4c592b9b-53ae-4fe6-e063-6294a90ae979
Type HUMAN OTC DRUG
Nonproprietary name vitamin E, lysine
Dosage form LIQUID
Route OPHTHALMIC
Labeler Guangzhou Mizi Biotechnology Co., LTD.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-06
Substance LYSINE; ASPARTIC ACID; OLIGOPEPTIDE-10; SODIUM HYALURONATE; .ALPHA.-TOCOPHEROL
Active strength .01; .02; .01; .001; .02 g/mL; g/mL; g/mL; g/mL; g/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 STYE EYE RELIEF SERUM
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LYSINE .01 g/mL ASPARTIC ACID .02 g/mL OLIGOPEPTIDE-10 .01 g/mL SODIUM HYALURONATE .001 g/mL .ALPHA.-TOCOPHEROL .02 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 84896-005-01 STYE EYE 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 84896-005-01 84896000501 30 mL in 1 BOTTLE (84896-005-01) 30 ml 2026-03-06 No No Current