Home NDC 67172-696-01 Clear Eyes Maximum Redness Relief
Product NDC 67172-696
Requested package NDC 67172-696-01
11-digit product format 671720696
Labeler code 67172
Product ID 67172-696_6dbafbc8-4288-4907-83f8-751de6885922
Type HUMAN OTC DRUG
Nonproprietary name Naphazoline Hydrochloride and Glycerin
Dosage form LIQUID
Route OPHTHALMIC
Labeler Prestige Brands Holdings, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-09-01
Substance NAPHAZOLINE HYDROCHLORIDE; GLYCERIN
Active strength .3; 5 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 Clear Eyes Maximum Redness Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength NAPHAZOLINE HYDROCHLORIDE .3 mg/mL GLYCERIN 5 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1235200 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 67172-696-01 Clear Eyes Maximum Redness Relief 30 mL in 1 BOTTLE, DROPPER LIQUID 30 6 67172-696-01 Clear Eyes Maximum Redness Relief 1 in 1 CARTON LIQUID 1 6 67172-696-02 Clear Eyes Maximum Redness Relief 1 in 1 CARTON LIQUID 1 6 67172-696-02 Clear Eyes Maximum Redness Relief 15 mL in 1 BOTTLE, DROPPER LIQUID 15 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded GLYCERIN ACTIVE INGREDIENT PDC6A3C0OX CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 NAPHAZOLINE HYDROCHLORIDE ACTIVE INGREDIENT MZ1131787D CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 GLYCERIN ACTIVE MOIETY PDC6A3C0OX CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 NAPHAZOLINE ACTIVE MOIETY H231GF11BV CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 BORIC ACID INACTIVE INGREDIENT R57ZHV85D4 CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 SODIUM BORATE INACTIVE INGREDIENT 91MBZ8H3QO CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67172-696 CLEAR EYES MAXIMUM REDNESS RELIEF (NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN) LIQUID [PRESTIGE BRANDS HOLDINGS, INC.] 6 Current NDC, Legacy NDC, 4 package rows 20250227_c3b0e344-68dd-4c35-bf46-744e612a5b15.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 25 of 25 · 486 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join REFRESH TEARS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 329d1fe0-4432-4565-b7b1-65666bd86526 2022-06-30 Warnings Exact identifier application number: M018 REFRESH Optive Mega-3 CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 Allergan, Inc. c5f2b3f2-2071-45bd-a010-67f848bc0233 2022-06-30 Warnings Exact identifier application number: M018 REFRESH P.M. MINERAL OIL, PETROLATUM Allergan, Inc. 24365d64-cd94-41cc-a7e1-033102d98114 2022-06-30 Warnings Exact identifier application number: M018 REFRESH PLUS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 0f6a4b4b-cde6-4518-84b5-ce997f1154a7 2022-06-28 Warnings Exact identifier application number: M018 CIRCLE K sterile eye drops TETRAHYDROZOLINE HCL Lil' Drug Store Products, Inc. 2c0e106c-16f6-ff4e-e063-6294a90a7dbb 2018-07-30 Warnings Exact identifier application number: M018 Lil Drug Store Sterile Eye Drops Redness Reliever TETRAHYDROZOLINE HCL Lil' Drug Store Products, Inc. 2c0ea35c-ac52-1043-e063-6394a90a061c 2018-04-30 Warnings Exact identifier application number: M018
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 67172-696-01 67172069601 1 BOTTLE, DROPPER in 1 CARTON (67172-696-01) / 30 mL in 1 BOTTLE, DROPPER 2010-09-01 0000-00-00 No No Current