GONIOTAIRE- hypromellose 2906 (4000 mpa.s) solution 
Altaire Pharmaceuticals Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Goniotaire

Altaire

Goniotaire

Hypromellose 2.5% Ophthalmic

Demulcent Solution

 15mL

NDC 59390-182-13

Drug Facts

Each mL Contains:

Active:

Hypromellose 25mg (2.5%):

Inactives:

Benzalkonium Chloride, Boric Acid, Edetate Disodium, Sodium Borate, Water for injection. Hydrochloric Acid and/or sodium hydroxide may be added to adjust pH (6.0 to 7.8).

NOTE: If this solution dries on optical surfaces, let them stand in cool water before cleansing.

INDICATIONS:

For professional use in gonioscopic examinations.

DIRECTIONS:

Fill gonioscopic prism with solution as necessary.

WARNINGS:

To avoid contamination do not touch tip of container to any surface. Replace cap after using. Not for use in conjunction with hot laser treatment. If solution changes color or becomes cloudy, do not use.

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.

STORAGE:

Store at room temperature 15°- 30°C (59°- 86°F).

PRINCIPAL DISPLAY PANEL

NDC 59390-182-13
Goniotaire
Hypromellose 2.5%
Ophthalmic Demulcent
Solution (Sterile)
½ fl oz (15mL)
sterile

PRINCIPAL DISPLAY PANEL
NDC 59390-182-13
Goniotaire 
Hypromellose 2.5% 
Ophthalmic Demulcent 
Solution (Sterile)
½ fl oz (15mL)
sterile

GONIOTAIRE 
hypromellose 2906 (4000 mpa.s) solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:59390-182
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPROMELLOSE 2906 (4000 MPA.S) (UNII: 5EYA69XGAT) (HYPROMELLOSE 2906 (4000 MPA.S) - UNII:5EYA69XGAT) HYPROMELLOSE 2906 (4000 MPA.S)25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
WATER (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID (UNII: QTT17582CB)  
May containSODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59390-182-131 in 1 CARTON01/18/2002
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/18/2002
Labeler - Altaire Pharmaceuticals Inc. (786790378)

Revised: 10/2022
Document Id: 3e98cefc-43d0-40bf-80be-651f17a39d4f
Set id: 9ebedd36-523a-4f92-8fe9-33beaf7288f9
Version: 3
Effective Time: 20221028
 
Altaire Pharmaceuticals Inc.