CLEAR EYES COMPLETE 7 SYMPTON RELIEF- hypromellose, naphazoline hydrochloride, polysorbate 80 and zinc sulfate liquid 
Prestige Brands Holdings, Inc.

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Clear Eyes Complete 7 Symptom Relief

Drug Facts

Active Ingredients

Hypromellose 0.20%

Purpose

Lubricant

Active Ingredients

Naphazoline Hydrochloride 0.025%

Purpose

Redness Reliever

Active Ingredients

Polysorbate 80 0.50%

Purpose

Lubricant

Active Ingredients

Zinc Sulfate 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 of container to any surface.
  • Replace cap after using.
  • Overuse of this product may produce 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 right away.

Directions

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

Other Information

Inactive Ingredients

calcium chloride, citric acid, edetate disodium, magnesium chloride, potassium chloride, purified water, sodium citrate, sodium chloride and sorbic acid.

Questions?

1-877-274-1787

www.cleareyes.com

PRINCIPAL DISPLAY PANEL

CLEAR
EYES ®
complete for
7 SYMPTOM RELIEF

ASTRINGENT
 LUBRICANT/REDNESS RELIEVER EYE DROPS
Sterile 0.5 FL oz (15 mL)

CLEAR
EYES ®
complete for 
7 SYMPTOM RELIEF
ASTRINGENT LUBRICANT/REDNESS RELIEVER EYE DROPS
Sterile 0.5 FL oz (15 mL)

CLEAR EYES COMPLETE 7 SYMPTON RELIEF 
hypromellose, naphazoline hydrochloride, polysorbate 80 and zinc sulfate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-707
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPROMELLOSES (UNII: 3NXW29V3WO) (HYPROMELLOSES - UNII:3NXW29V3WO) HYPROMELLOSES.5 mg  in 1 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE.0625 mg  in 1 mL
POLYSORBATE 80 (UNII: 6OZP39ZG8H) (POLYSORBATE 80 - UNII:6OZP39ZG8H) POLYSORBATE 801.25 mg  in 1 mL
ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION.625 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-707-011 in 1 BOX06/12/2013
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 DrugM01806/12/2013
Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 10/2024
Document Id: 8567fbd9-dc22-41b6-807f-03e46295073b
Set id: 7376b806-8e34-4c30-a902-1354edbde771
Version: 7
Effective Time: 20241025
 
Prestige Brands Holdings, Inc.