POLYVINYL ALCOHOL EYE DROPS 1,4 % W/V- polyvinyl alcohol eye drops 1,4 % w/v for solution 
Aurolab

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Active ingredient

Polyvinyl Alcohol Eye Drops 1.4 % w/v

DIRECTIONS FOR USE

INACTIVE INGREDIENT

1.Boric acid

2.Calcium chloride

3.Glycerin
4.Magnesium chloride

5.Mannitol

6.Potassium chloride

7.Purified water

8.Stablized oxy cholro complex

9.Sodium tetra borate
10.Sodium hyaluronate

11.Sodium citrate

Tamper Protection

Use

For use as a lubricant to prevent further irritation or to relieve dryness of the eye

Questions

Call. 1-800-103-7321
E-mail : info@aurolab.com
Web : www.aurolab.com

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away

Stop use and ask a doctor if

  1. If you experience eye pain
  2. change in vision
  3. Continued Redness or irritaion of teh eye
  4. Condition worsens or persists for mroe than 72 hours

Do not use

1.If you are sensitive to any ingredient in this product
2.If solution changes color or becomes cloudy

Warnings

For external use only

Indication & usage

Do not touch the nozzle tip to any surface since this may contaminate the solution
Remove contact lenses before use Should not use at the same time as other ophthalmic drugs
Replace cap after using

Dose

Instill 1 or 2 drops in the affected eyes as needed

Eye lubricant

Eye lubricant

Carton

PVA

POLYVINYL ALCOHOL EYE DROPS 1,4 % W/V 
polyvinyl alcohol eye drops 1,4 % w/v for solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16030-201
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990) POLYVINYL ALCOHOL, UNSPECIFIED5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
POVIDONE (UNII: FZ989GH94E)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:16030-201-055 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/20/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01809/20/2022
Labeler - Aurolab (677319965)
Establishment
NameAddressID/FEIBusiness Operations
Aurolab677319965manufacture(16030-201)

Revised: 1/2024
Document Id: 0ff5311d-8d43-7272-e063-6294a90aaae9
Set id: e8e09719-6e06-612b-e053-2995a90a79fc
Version: 7
Effective Time: 20240127
 
Aurolab