GNP EYEDROPS MAXIMUM REDNESS RELIEF- glycerin, naphazoline hcl solution 
AmerisourceBergen

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GNP Eye Drops Maximum Redness Relief (PLD)

Active ingredients

Glycerin.....0.5%

Naphazoline HCl...0.03%

Purpose

Glycerin.....Lubricant

Naphazoline HCl...Redness reliever

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 may producte increased redness of the eye
  • pupils may become enlarged temporarily

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 or persists 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

Inactive ingredients

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

Questions or comments?

Call 1-866-627-4278

carton

GNP EYEDROPS MAXIMUM REDNESS RELIEF 
glycerin, naphazoline hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-603
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.03 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
WATER (UNII: 059QF0KO0R)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-603-051 in 1 CARTON09/05/2019
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 DrugM01809/05/2019
Labeler - AmerisourceBergen (007914906)
Registrant - K.C. Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
K.C. Pharmaceuticals, Inc.174450460manufacture(46122-603) , pack(46122-603) , label(46122-603)

Revised: 12/2023
Document Id: 0d291a5f-b635-380c-e063-6394a90a0310
Set id: 9b594424-08ad-c006-e053-2a95a90af91e
Version: 3
Effective Time: 20231223
 
AmerisourceBergen