CLEAR EYES ADVANCED DRY AND ITCHY- glycerin solution/ drops 
Prestige Brands Holdings, Inc.

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Clear eyes ADVANCED Dry and Itchy Eye Drops

Drug Facts

Active ingredient

Glycerin 0.25%

Purpose

Lubricant

Uses

Warnings

For external use only

Do not use

if solution changes color or becomes cloudy

When using this product

  • to avoid contamination, do not touch tip to any surface
  • replace cap after using

Stop use and ask a doctor if

  • you experience eye pain
  • you experience changes in vision
  • you experience continued rednes 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 or 2 drops in the affected eye(s) as needed.

Other information

Inactive ingredients

boric acid, phosphatidylcholine, polyhexanide, purified water, sodium borate, sodium chloride, sodium hyaluronate, tocopherol acetate

Questions?

1-877-274-1787 Cleareyes.com

PRINCIPAL DISPLAY PANEL

Clear eyes ADVANCED

DRY & ITCHY RELIEF

Glyercin / Lubricant Eye Drops

Sterile             0.5 FL OZ (15 mL)

PRINCIPAL DISPLAY PANEL

Clear eyes ADVANCED™
DRY & ITCHY RELIEF

Glyercin / Lubricant Eye Drops 

Sterile	0.5 FL OZ (15 mL)

CLEAR EYES ADVANCED DRY AND ITCHY 
glycerin solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-502
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
POLIHEXANIDE (UNII: 322U039GMF)  
PHOSPHATIDYLCHOLINE TRANSLOCATOR ABCB4 (UNII: 9EI49ZU76O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-502-151 in 1 CARTON02/15/201912/31/2025
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01802/15/201912/31/2025
Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 10/2024
Document Id: 85fe82e1-4926-4b07-8cee-31b0a15b14e8
Set id: 336ae239-0324-4975-8701-0c72e5540d51
Version: 3
Effective Time: 20241025
 
Prestige Brands Holdings, Inc.