CLEAR EYES PURE RELIEF MULTISYMPTOM- glycerin solution/ drops
Prestige Brands Holdings, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Clear Eyes Pure Relief Multi-symptom

Drug Facts

Active ingredients

Phenylephrine hydrochloride 0.10%

Glycerin 0.25%

Hypromellose 0.30%

Purpose

Redness reliever

Lubricant

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

Warnings

For external use only

Do not use

if solution changes color or becomes cloudy

Ask a doctor before use if you have

narrow angle glaucoma

When using this product

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

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.

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

Directions

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

Other information

store at room temperature
remove contact lenses before using

Inactive ingredients

citric acid, purified water, sodium chloride, sodium citrate

Questions?

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

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)

CLEAR EYES PURE RELIEF MULTISYMPTOM
glycerin solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67172-501
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	1 mg in 1 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	2.5 mg in 1 mL
HYPROMELLOSES (UNII: 3NXW29V3WO) (HYPROMELLOSES - UNII:3NXW29V3WO)	HYPROMELLOSES	3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:67172-501-10	1 in 1 CARTON	12/15/2015	09/30/2020
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part349	12/15/2015	09/30/2020

Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 12/2019

Document Id: 2638cde8-20c4-4dff-a5fb-721a72f41058

Set id: 38f5adea-d621-466d-a3fa-557e32eab4d3

Version: 3

Effective Time: 20191224

Prestige Brands Holdings, Inc.