GONIOTAIRE (hypromellose 2906- 4000 mpa.s solution

Goniotaire by

Drug Labeling and Warnings

Goniotaire by is a Prescription medication manufactured, distributed, or labeled by Altaire Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

GONIOTAIRE 
hypromellose 2906 (4000 mpa.s) solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 59390-182
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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 Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM BORATE (UNII: 91MBZ8H3QO)
WATER (UNII: 059QF0KO0R)

Other Ingredients
Ingredient Kind	Ingredient Name	Quantity
May contain	HYDROCHLORIC ACID (UNII: QTT17582CB)
May contain	SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59390-182-13	1 in 1 CARTON	01/18/2002
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		01/18/2002

Labeler - Altaire Pharmaceuticals Inc. (786790378)