CVS ASTRINGENT EYE- tetrahydrozoline hcl, zinc sulfate solution/ drops 
CVS Pharmacy, Inc.

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CVS Astringent Eye Drops (PLD)

​Active ingredients

Tetrahydrozoline HCl 0.05%

Zinc sulfate 0.25%

​Purpose

Tetrahydrozoline HCl...Redness Reliever

Zinc sulfate...Astringent

Uses

Warnings

For external use only

Ask a doctor before use if you have narrow angle glaucoma

When using this product

  • pupils may become enlarged temporarily
  • to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
  • if solution changes color or becomes cloudy, do not use
  • overuse may produce increased redness of the eye
  • remove contact lens before using

Stop use and ask a doctor if you experience

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Other information

Store at 15°-30°C (59°-86°F)

Inactive ingredients

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium chloride, and sodium citrate

Carton

CVS ASTRINGENT EYE 
tetrahydrozoline hcl, zinc sulfate solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-611
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE50 mg  in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION250 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-611-011 in 1 BOX11/01/2007
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 DrugM01811/01/2007
Labeler - CVS Pharmacy, Inc. (062312574)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(69842-611) , label(69842-611) , pack(69842-611)

Revised: 12/2023
Document Id: 0d378048-39d5-421b-e063-6294a90ac848
Set id: 07e1a56b-fdad-408d-bf5a-7a0144ece131
Version: 4
Effective Time: 20231223
 
CVS Pharmacy, Inc.