Home NDC 55651-005 Medics Choice Eye Drops Original Redness Reliever
Product NDC 55651-005
11-digit product format 556510005
Labeler code 55651
Product ID 55651-005_4748ccb8-2816-8c8c-e063-6294a90a908c
Type HUMAN OTC DRUG
Nonproprietary name tetrahydrozoline hydrochloride
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler KC Pharmaceuticals, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2003-08-28
Substance TETRAHYDROZOLINE HYDROCHLORIDE
Active strength .5 mg/mL
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 Medics Choice Eye Drops Original Redness Reliever
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TETRAHYDROZOLINE HYDROCHLORIDE .5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0YZT43HS7D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1052943 Internal RxNorm 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 55651-005-01 Medics Choice Eye Drops Original Redness Reliever 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 4 55651-005-01 Medics Choice Eye Drops Original Redness Reliever 1 in 1 CARTON SOLUTION/ DROPS 1 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded TETRAHYDROZOLINE HYDROCHLORIDE ACTIVE INGREDIENT 0YZT43HS7D EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 TETRAHYDROZOLINE ACTIVE MOIETY S9U025Y077 EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 BORIC ACID INACTIVE INGREDIENT R57ZHV85D4 EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 SODIUM BORATE INACTIVE INGREDIENT 91MBZ8H3QO EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R EYE DROPS REGULAR (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55651-005 MEDICS CHOICE EYE DROPS ORIGINAL REDNESS RELIEVER (TETRAHYDROZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20240110_e42cb1bf-b985-4a1b-9a9b-ac27c2a5d7be.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 55651-005-01 55651000501 1 BOTTLE, DROPPER in 1 CARTON (55651-005-01) / 15 mL in 1 BOTTLE, DROPPER 2003-08-28 0000-00-00 No No Current