GLITCH ADVANCED RELIEF EYE DROPS- polyethylene glycol 400, tetrahydrozoline hcl solution/ drops 
Misemer Pharmaceutical, Inc

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Glitch Advanced Relief Eye Drops 15mL (PLD)

Active ingredients

Polyethylene glycol 400 1%

Tetrahydrozoline HCI 0.05%

Purposes

Lubricant

Redness reliever

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 (1-800-222-1222) 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, dextran, edetate disodium, povidone, purified water, sodium borate, sodium chloride

Questions or comments?

Call 1-662-993-9625 Mon-Fri

9 am - 5 pm EST

Glitch Advanced Relief Eye Drops 15mL

Glitch Advanced Relief Eye Drops 15mL

GLITCH ADVANCED RELIEF EYE DROPS 
polyethylene glycol 400, tetrahydrozoline hcl solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0276-0801
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4001 g  in 100 mL
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.05 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
DEXTRAN 70 (UNII: 7SA290YK68)  
POVIDONE (UNII: FZ989GH94E)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0276-0801-151 in 1 BOX08/21/2023
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 DrugM01808/21/2023
Labeler - Misemer Pharmaceutical, Inc (784121365)
Registrant - KC Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
KC Pharmaceuticals, Inc.174450460manufacture(0276-0801) , pack(0276-0801) , label(0276-0801)

Revised: 12/2023
Document Id: 0d3842c0-149e-b681-e063-6394a90a52ed
Set id: 03778509-3374-2168-e063-6294a90a9505
Version: 2
Effective Time: 20231223
 
Misemer Pharmaceutical, Inc