Advanced Eye Relief Dry Eye Rejuvenation description, usages, side effects, indications, overdosage, supplying and lots more!

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Advanced Eye Relief Dry Eye Rejuvenation

Bausch & Lomb Incorporated

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Glycerin (0.3%)

Propylene glycol (1.0%)

Lubricant

Lubricant

  • •temporary relief of burning and irritation due to dryness of the eye
  • •prevents further irritation

Do not use

  • •if solution changes color or becomes cloudy

When using this product

  • •do not touch tip of container to any surface to avoid contamination
  • •remove contact lenses before using
  • •replace cap after use

Stop use and ask a doctor if

  • •you experience eye pain, changes in vision, continued redness or irritation of the eye
  • •condition worsens or persists for more than 72 hours

Keep out of reach of children.

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

  • •Instill 1 or 2 drops in the affected eye(s) as needed
  • •store at 15°-25°C (59°-77°F)
  • •keep tightly closed
  • •use before expiration date marked on the carton and bottle

benzalkonium chloride (0.01%) boric acid, edetate disodium, potassium chloride, purified water, sodium borate, sodium chloride. Hydrochloric acid and/or sodium hydroxide may be used to adjust pH.

Toll Free Product Information or to Report a Serious Side Effect Associated with use of this product Call: 1-800-553-5340

Package/Label Principal Display Panel

Bausch & Lomb

ADVANCED

Eye ReliefTM

Dry Eye

Rejuvenation

LUBRICANT EYE DROPS

Fast relief from age-related dry eyes

Replenishes tears

Refreshes eyes

STERILE 0.5 FL OZ (15 mL)

Advanced Eye Relief Dry Eye Rejuvenation

glycerin propylene glycol SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24208-454
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GLYCERIN 3 mg
propylene glycol Propylene Glycol 10 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
BORIC ACID
EDETATE DISODIUM
potassium chloride
water
SODIUM BORATE
SODIUM CHLORIDE
HYDROCHLORIC ACID
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:24208-454-32 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-09-01


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Be sure to consult your doctor before taking any medication!
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