IVIZIA LUBRICANT EYE FOR SEVERE NIGHT DRY EYES- povidone solution, gel forming / drops 
Similasan Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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iVizia Lubricant Eye Gel for Severe Night Dry Eyes

Active Ingredient

Povidone 0.5%

Purpose

Eye lubricant

Uses

(one or more of these)

Warnings:

Keep out of reach of children.

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

When using this product

  • Rare possibility of mild eye irritation and ocular redness. In such cases, contact lens wearers should remove their contact lenses.
  • You might experience bothersome symptoms such as a burning sensation, stinging sensation, foreign body sensation in the eye and blurred vision for a short time.

Directions:

Gel is particularly suited for severe dry eye or nighttime use.

Inactive Ingredients

Carbomer, Purified water, Sodium hyaluronate, Sodium hydroxide, Sorbitol, Trehalose

Questions?

1-800-240-9780 or info@ivizia.com.

Principle Display Panel

iVizia
Lubricant Eye Gel
For Severe/Night Dry Eyes
0.014 OZ (0.4g) each

30 sterile single-use vials

Principle Display Panel
iVizia
Lubricant Eye Gel
For Severe/Night Dry Eyes
0.014 OZ (0.4g) each
30 sterile single-use vials

IVIZIA LUBRICANT EYE FOR SEVERE NIGHT DRY EYES 
povidone solution, gel forming / drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59262-701
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE2.5 mg  in 0.5 g
Inactive Ingredients
Ingredient NameStrength
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
WATER (UNII: 059QF0KO0R)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SORBITOL (UNII: 506T60A25R)  
TREHALOSE (UNII: B8WCK70T7I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59262-701-1230 in 1 CARTON10/14/2021
10.4 g in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34910/14/2021
Labeler - Similasan Corporation (111566530)

Revised: 8/2023
Document Id: 941cec6d-9879-4153-b834-e12008196994
Set id: 50d9cc60-5735-4546-b183-d2eb4906c603
Version: 3
Effective Time: 20230814
 
Similasan Corporation