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

----------

Clear Eyes Complete

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
ASTRINGENT/LUBRICANT/REDNESS RELIEVER EYE DROPS

Sterile 0.5 FL OZ (15 mL)

PRINCIPAL DISPLAY PANEL
Clear Eyes Complete
0.5 FL OZ (15 mL)

CLEAR EYES COMPLETE 7 SYMPTOM RELIEF 
hypromellose and naphazoline hydrochloride and polysorbate 80 and zinc sulfate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-595
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC SULFATE (UNII: 89DS0H96TB) (ZINC - UNII:J41CSQ7QDS) ZINC SULFATE.625 mL  in 1 mL
POLYSORBATE 80 (UNII: 6OZP39ZG8H) (POLYSORBATE 80 - UNII:6OZP39ZG8H) POLYSORBATE 801.25 mL  in 1 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE.0625 mL  in 1 mL
HYPROMELLOSE (UNII: 3NXW29V3WO) (HYPROMELLOSE - UNII:3NXW29V3WO) HYPROMELLOSE.5 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
CITRIC ACID (UNII: 2968PHW8QP)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SORBIC ACID (UNII: X045WJ989B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-595-011 in 1 BOX
115 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34903/01/2010
Labeler - Prestige Brands Holdings, Inc. (159655021)
Establishment
NameAddressID/FEIBusiness Operations
Altaire Pharmaceuticals Inc.786790378MANUFACTURE

Revised: 8/2010
Document Id: 183db81c-7986-4626-88a6-341db9be25ce
Set id: 9a1ce5e2-c3da-424d-b754-cf2de8c655e3
Version: 1
Effective Time: 20100815
 
Prestige Brands Holdings, Inc.