CLEAR EYES NIGHTTIME- glycerin solution/ drops 
Prestige Brands Holdings, Inc.

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Clear Eyes Nighttime

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.

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 produce 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

Put 1 to 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 ®
NIGHTTIME
Restoring Drops

Glycerin / Lubricant Eye Drops

Sterile             0.5 FL OZ (15 mL)

Clear eyes ®
NIGHTTIME 
Restoring Drops

Glycerin / Lubricant Eye Drops 

Sterile		0.5 FL OZ (15 mL)

CLEAR EYES NIGHTTIME 
glycerin solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-505
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)  
PHOSPHATIDYLCHOLINE, SOYBEAN (UNII: 1T6N4D9YV6)  
POLIHEXANIDE (UNII: 322U039GMF)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-505-151 in 1 CARTON01/08/2024
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 DrugM01801/08/2024
Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 1/2024
Document Id: 5adddd37-bc93-4b75-8f9c-340a6b010bb9
Set id: af75e2f7-81dd-43e0-a390-b52bbfbebf62
Version: 3
Effective Time: 20240111
 
Prestige Brands Holdings, Inc.