Home NDC 66715-7010 Cleareyes Redness Relief
Product NDC 66715-7010
11-digit product format 667157010
Labeler code 66715
Product ID 66715-7010_0c8f4454-0523-b87a-e063-6394a90aa9b7
Type HUMAN OTC DRUG
Nonproprietary name Naphazoline Hydrochloride and Glycerin
Dosage form LIQUID
Route OPHTHALMIC
Labeler Lil' Drug Store Products, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2000-11-02
Substance NAPHAZOLINE HYDROCHLORIDE; GLYCERIN
Active strength .00012; .0025 mg/mL; mg/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
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 Cleareyes Redness Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength NAPHAZOLINE HYDROCHLORIDE .00012 mg/mL GLYCERIN .0025 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination MZ1131787D Internal UNII lookup PDC6A3C0OX Internal UNII 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 66715-7010-3 Cleareyes Redness Relief 1 in 1 PACKAGE LIQUID 1 4 66715-7010-3 Cleareyes Redness Relief 6 mL in 1 BOTTLE, DROPPER LIQUID 6 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66715-7010 CLEAREYES REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [LIL' DRUG STORE PRODUCTS, INC.] 4 Current NDC, Legacy NDC, 2 package rows 20231216_39e4ab2b-ae12-4339-b219-109cf0f7f06a.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 66715-7010-3 66715701003 1 BOTTLE, DROPPER in 1 PACKAGE (66715-7010-3) / 6 mL in 1 BOTTLE, DROPPER 2020-01-15 0000-00-00 No No Current