FDA.reportPublic FDA data

Clear Eyes Pure Relief Multisymptom

Manufacturer
Prestige Brands Holdings, Inc.
Effective date
2019-12-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:49:56

Label at a glance#

ProductClear Eyes Pure Relief Multisymptom
Active ingredientPHENYLEPHRINE HYDROCHLORIDE, GLYCERIN, HYPROMELLOSES
Label structure10 sections

Indications and uses

relieves redness of the eye due to minor eye irritations for the temporary relief of burning and irritation due to dryness of the eye for use as a protectant against further irritation or dryness of the eye

Dosage and administration

Instill 1 to 2 drops in the affected eye(s)up to four times daily.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Phenylephrine hydrochloride 0.10%

Glycerin 0.25%

Hypromellose 0.30%

Purpose

OTC - PURPOSE SECTION

Redness reliever

Lubricant

Lubricant

Uses

INDICATIONS & USAGE SECTION

  • relieves redness of the eye due to minor eye irritations
  • for the temporary relief of burning and irritation due to dryness of the eye
  • for use as a protectant against further irritation or dryness of the eye

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if solution changes color or becomes cloudy

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

narrow angle glaucoma

When using this product

OTC - WHEN USING SECTION

  • to avoid contamination, do not touch tip to any surface
  • replace cap after using
  • overuse may cause increased redness of the eye
  • pupils may become enlarged temporarily

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you experience eye pain
  • you experience changes in vision
  • you experience continued redness or irritation of the eye
  • the condition worsens
  • symptoms last for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Instill 1 to 2 drops in the affected eye(s)up to four times daily.

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature
  • remove contact lenses before using

Inactive ingredients

INACTIVE INGREDIENT SECTION

citric acid, purified water, sodium chloride, sodium citrate

Questions?

OTC - QUESTIONS SECTION

1-877-274-1787 www.cleareyes.com

©2017 Dist. by Medtech Products Inc.
Tarrytown, NY 10591
A Prestige Brands Company
Made in Italy

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Clear Eyes®Pure Relief™ 
MULTI-SYMPTOM
Lubricant/Redness Reliever Eye Drops
0.34 FL OZ (10 mL)

PRINCIPAL DISPLAY PANEL Clear Eyes®Pure Relief™ MULTI-SYMPTOM Lubricant/Redness Reliever Eye Drops 0.34 FL OZ (10 mL)PRINCIPAL DISPLAY PANEL Clear Eyes®Pure Relief™ MULTI-SYMPTOM Lubricant/Redness Reliever Eye Drops 0.34 FL OZ (10 mL)

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67172-501-10ML - Milliliter67172-501e1a9646e-17a3-4e1c-ab73-54603f7eed0e12019-02-13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67172-50167172-501-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENYLEPHRINE HYDROCHLORIDE04JA59TNSJACTIB
GLYCERINPDC6A3C0OXACTIB
HYPROMELLOSES3NXW29V3WOACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM CITRATE1Q73Q2JULRIACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2638cde8-20c4-4dff-a5fb-721a72f4105838f5adea-d621-466d-a3fa-557e32eab4d32019-12-24WarningsExact identifier
spl id: 2638cde8-20c4-4dff-a5fb-721a72f41058
spl set id: 38f5adea-d621-466d-a3fa-557e32eab4d3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.