Activeingredient

Sodium Chloride 5%

Purpose

Hypertonicity Agent

Use

For the temporary relief of corneal edema.

Warnings

For use in the eyesonly

Save box for complete information

Do not use

except under the advice and supervision of a doctor.
if solution changes color or becomes cloudy.

When using this product

keep tightly closed.
to avoid contamination, do not touch tip of container to any surface.
replace cap immediately after each use.
this product may cause temporary burning and irritation on being instilled into the eye.

Stop use and ask a doctor if

you experience eye pain.
changes in your vision occur.
continued redness or irritation of the eye persists.
condition worsens or persists.

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) every 3 to 4 hours, or as directed by a doctor.

Other information

replace cap after using and keep tightly closed.
store at 15° to 30°C (59° to 86°F).
remove contact lenses before using.

Inactive ingredients

Boric Acid, Hypromellose, Methylparaben, Propylene Glycol, Proplyparaben, Sodium Borate, and Water for injection. Sodium Hydroxide and/or Hydrochloric Acid may be added to adjust pH.

Questions?

1 (800) 258-2471
9am– 5pm EST Monday - Friday

PRINCIPAL DISPLAY PANEL

iSolutionsActivEyesAltachlore5% SolutionSodium ChlorideHypertonicity OphthalmicSolution5%Sterile
15mLNET WT (1/2 FL OZ)

PRINCIPAL DISPLAY PANEL
iSolutions
ActivEyes
Altachlore
5% Solution
Sodium Chloride
Hypertonicity Ophthalmic
Solution 5%
Sterile 15mL
NET WT (1/2 FL OZ)

ALTACHLORE SODIUM CHLORIDE HYPERTONICITY
sodium chloride solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59390-183
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	50 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
BORIC ACID (UNII: R57ZHV85D4)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM BORATE (UNII: 91MBZ8H3QO)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROCHLORIC ACID (UNII: QTT17582CB)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:59390-183-13	1 in 1 CARTON	09/24/2002
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	09/24/2002

Labeler - Altaire Pharmaceuticals Inc. (786790378)

Name	Address	ID/FEI	Business Operations
Establishment
Altaire Pharmaceuticals Inc.		786790378	manufacture(59390-183)

Altachlore Sodium Chloride Hypertonicity Ophthalmic Solution