CLEAR EYES REDNESS RELIEF- naphazoline hydrochloride and glycerin liquid 
Preferred Pharmaceuticals 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 Redness Relief

Clear Eyes Redness Relief

Drug Facts

Active Ingredients

Glycerin 0.25%

Purpose

Lubricant

Active Ingredients

Naphazoline hydrochloride 0.012%

Purpose

Redness Reliever

Uses

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

pupils may become enlarged temporarily
overuse may produce increased redness of the eye
remove contact lenses before using
to avoid contamination, do not touch tip of container 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 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 4 times daily.

Other Information

store at room temperature
 

Inactive Ingredients

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate

Questions?

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

Clear Eyes Redness Relief, Handy Pocket Pal

Drug Facts

Active Ingredients

Glycerin 0.25%

Purpose

Lubricant

Active Ingredients

Naphazoline hydrochloride 0.012%

Purpose

Redness Reliever

Uses

Relieves redness of the eye due to minor eye irritations.
For use as a protectant against further irritation or to relieve dryness of the eye.
Temporarily relieves burning and irritation due to 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 & 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 Between 20° -25°C (68° -77°F)
Remove contact lenses before using.

Relabeled By: Preferred Pharmaceuticals Inc.

Inactive Ingredients

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate

Questions?

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

PRINCIPAL DISPLAY PANEL


Clear eyes REDNESS RELIEF
LUBRICANT/REDNESS RELIEVER EYE DROPS
Sterile 0.5 FL OZ (15 mL)

Clear Eyes
CLEAR EYES REDNESS RELIEF 
naphazoline hydrochloride and glycerin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-7611(NDC:67172-797)
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.12 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68788-7611-11 in 1 BOX02/07/2020
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34902/07/2020
Labeler - Preferred Pharmaceuticals Inc. (791119022)
Registrant - Preferred Pharmaceuticals Inc. (791119022)
Establishment
NameAddressID/FEIBusiness Operations
Preferred Pharmaceuticals Inc.791119022RELABEL(68788-7611)

Revised: 4/2023
Document Id: 39c3a811-fdab-49bc-9e99-1df3136cc2c8
Set id: ac87a2d0-56f7-4654-b660-17de22bd29f2
Version: 4
Effective Time: 20230426
 
Preferred Pharmaceuticals Inc.