GNP EYE DROPS SEASONAL RELIEF- tetrahydrozoline hcl, zinc sulfate solution 
AmerisourceBergen

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GNP Eye Drops Seasonal Relief (PLD)

Active ingredients

Tetrahydrozoline HCl....0.05%

Zinc sulfate.....0.25%

Purposes

Tetrahydrozoline HCl......Redness reliever

Zinc sulfate......Astringent

Use

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 (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 15º-30ºC (59º-86ºF)

Inactive ingredients

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

Questions or comments?

Call 1-888-527-4276

Carton

GNP EYE DROPS SEASONAL RELIEF 
tetrahydrozoline hcl, zinc sulfate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-602
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.05 g  in 100 mL
ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION0.25 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
WATER (UNII: 059QF0KO0R)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-602-051 in 1 CARTON08/28/2019
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 DrugM01808/28/2019
Labeler - AmerisourceBergen (007914906)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
K.C. Pharmaceuticals, Inc.174450460manufacture(46122-602) , pack(46122-602) , label(46122-602)

Revised: 12/2023
Document Id: 0d291a5f-b634-380c-e063-6394a90a0310
Set id: 9b11b129-7787-8a9d-e053-2995a90a45fe
Version: 3
Effective Time: 20231223
 
AmerisourceBergen