Home NDC 55651-024 Medics Choice Eye Drops Seasonal Relief
Product NDC 55651-024
11-digit product format 556510024
Labeler code 55651
Product ID 55651-024_4748cbbd-a95a-77cf-e063-6294a90a92b5
Type HUMAN OTC DRUG
Nonproprietary name tetrahydrozoline hydrochloride, zinc sulfate
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler KC Pharmaceuticals, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2003-10-23
Substance ZINC SULFATE; TETRAHYDROZOLINE HYDROCHLORIDE
Active strength 2.5; .5 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Seasonal Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC SULFATE 2.5 mg/mL TETRAHYDROZOLINE HYDROCHLORIDE .5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 89DS0H96TB Internal UNII lookup 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 1043249 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 55651-024-01 Medics Choice Eye Drops Seasonal Relief 1 in 1 CARTON SOLUTION/ DROPS 1 6 55651-024-01 Medics Choice Eye Drops Seasonal Relief 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded TETRAHYDROZOLINE HYDROCHLORIDE ACTIVE INGREDIENT 0YZT43HS7D EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 ZINC SULFATE ACTIVE INGREDIENT 89DS0H96TB EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 TETRAHYDROZOLINE ACTIVE MOIETY S9U025Y077 EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 ZINC ACTIVE MOIETY J41CSQ7QDS EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 BORIC ACID INACTIVE INGREDIENT R57ZHV85D4 EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 SODIUM CITRATE INACTIVE INGREDIENT 1Q73Q2JULR EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R EYE DROPS AC (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55651-024 MEDICS CHOICE EYE DROPS SEASONAL RELIEF (TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE) SOLUTION/ DROPS [KC PHARMACEUTICALS, INC.] 5 Current NDC, Legacy NDC, 2 package rows 20240110_92bd8cb4-90ad-4a47-afa4-30d1fa658d62.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 · 499 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 55651-024-01 55651002401 1 BOTTLE, DROPPER in 1 CARTON (55651-024-01) / 15 mL in 1 BOTTLE, DROPPER 2003-10-23 0000-00-00 No No Current