Home NDC 61715-212 Preferred Plus Pharmacy Redness Relief Eye Drops
Product NDC 61715-212
11-digit product format 617150212
Labeler code 61715
Product ID 61715-212_474a06ff-a21e-2ca2-e063-6394a90a7910
Type HUMAN OTC DRUG
Nonproprietary name tetrahydrozoline HCl
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Kinray
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-07-01
Substance TETRAHYDROZOLINE HYDROCHLORIDE
Active strength .05 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 61715-212-01 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 61715-212-01 f5e01cc5f278…a2eaf40c39c3…
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 Preferred Plus Pharmacy Redness Relief Eye Drops
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TETRAHYDROZOLINE HYDROCHLORIDE .05 g/100mL
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 61715-212-01 Preferred Plus Pharmacy Redness Relief Eye Drops 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 6 61715-212-01 Preferred Plus Pharmacy Redness Relief Eye Drops 1 in 1 CARTON SOLUTION/ DROPS 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61715-212 PREFERRED PLUS PHARMACY REDNESS RELIEF EYE DROPS (TETRAHYDROZOLINE HCL) SOLUTION/ DROPS [KINRAY] 4 Current NDC, Legacy NDC, 2 package rows 20231224_9ffd67c4-b5c1-d587-e053-2a95a90ae3d0.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 61715-212-01 61715021201 1 BOTTLE, DROPPER in 1 CARTON (61715-212-01) / 15 mL in 1 BOTTLE, DROPPER 2020-07-01 0000-00-00 No No Current