QUALITY CHOICE EYE DROPS MOISTURIZING RELIEF- dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline hcl solution 
Chain Drug Marketing Association, Inc.

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Quality Choice Eye Drops Moisturizing Relief (PLD)

Active ingredients

Dextran 70......0.1%

Polyethylene glycol 400.....1%

Povidone.....1%

Tetrahydrozoline HCl.....0.05%

Purpose

Dextran 70......Eye lubricant

Polyethylene glycol 400.....Eye lubricant

Povidone.....Eye lubricant

Tetrahydrozoline HCl.....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 proffessional 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 15º-30ºC (59º-86ºF)

Inactive ingredients

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

carton

QUALITY CHOICE EYE DROPS MOISTURIZING RELIEF 
dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-376
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 700.1 g  in 100 mL
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.05 g  in 100 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE1 g  in 100 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4001 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-376-151 in 1 CARTON01/05/2020
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 DrugM01801/05/2020
Labeler - Chain Drug Marketing Association, Inc. (011920774)
Registrant - K.C. Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
K.C. Pharmaceuticals, Inc.174450460manufacture(63868-376) , pack(63868-376) , label(63868-376)

Revised: 12/2023
Document Id: 0d2a8ad3-bddc-ab01-e063-6294a90aeb6c
Set id: 9b71c41d-8451-2fc6-e053-2995a90a5715
Version: 2
Effective Time: 20231223
 
Chain Drug Marketing Association, Inc.