Xpect Buffered Eyewash Sterile Isotonic description, usages, side effects, indications, overdosage, supplying and lots more!

Xpect Buffered Eyewash Sterile Isotonic

Cintas
Horizon Pharmaceuticals, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Xpect Buffered Eyewash Sterile Isotonic Solution

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purified water, 98.525%

Purpose

eyewash

Uses

for irrigating the eye to help relieve irritation, discomfort, burning, stinging, smarting, or itching by removing loose foreign material, air pollutants (smog or pollen), or chlorinated water.

Warnings

  • to avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
  • obtain immediate medical treatment for all open wounds in or near the eyes

Do not use

  • if solution changes color or becomes cloudy
  • with contact lenses
  • for injection

Stop use and ask a doctor if

  • you experience eye pain, changes in vision, continued redness, or irritation
  • condition worsens or persists

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Twist top to remove.
  • Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle

Inactive ingredients

benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

PRINCIPAL DISPLAY PANEL - 1 fl oz Bottle Label

Buffered
Eyewash

STERILE ISOTONIC
SOLUTION 1 fl oz

PRINCIPAL DISPLAY PANEL - 1 fl oz Bottle Label

Xpect Buffered Eyewash Sterile Isotonic

Water SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42961-301
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
water 0.98 mL

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
EDETATE DISODIUM
SODIUM CHLORIDE
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Sodium Phosphate, Monobasic, Monohydrate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE, UNIT-DOSE
2 NDC:42961-301-20 4 in 1 BOX, UNIT-DOSE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-10-01


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