CLEAR EYES PURE RELIEF MULTISYMPTOM- glycerin solution/ drops

Clear Eyes Pure Relief Multisymptom by

Drug Labeling and Warnings

Clear Eyes Pure Relief Multisymptom by is a Otc medication manufactured, distributed, or labeled by Prestige Brands Holdings, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Phenylephrine hydrochloride 0.10%

Glycerin 0.25%

Hypromellose 0.30%

Purpose

Redness reliever

Lubricant

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

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

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part349	12/15/2015	09/30/2020

Labeler - Prestige Brands Holdings, Inc. (159655021)