Home NDC 87770-001 VitaPhyte Redness Reliever Lubricant Eye Drops
Product NDC 87770-001
11-digit product format 877700001
Labeler code 87770
Product ID 87770-001_53d4e9b0-c9a1-797a-e063-6294a90ad0cf
Type HUMAN OTC DRUG
Nonproprietary name Redness Reliever Lubricant Eye Drops
Dosage form SOLUTION
Route OPHTHALMIC
Labeler Guangzhou Liyan Cosmetics Technology Co., Ltd.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-05
Substance TETRAHYDROZOLINE; POLYETHYLENE GLYCOL 400
Active strength 5; 1 mg/100g; g/100g
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 VitaPhyte Redness Reliever Lubricant Eye Drops
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TETRAHYDROZOLINE 5 mg/100g POLYETHYLENE GLYCOL 400 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination S9U025Y077 Internal UNII lookup B697894SGQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 996209 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 6 of 25 · 494 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 87770-001-01 87770000101 .15 g in 1 BOX (87770-001-01) 2026-06-03 No No Current