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

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Advanced Eye Relief/ Dry Eye/ Rejuvenation Lubricant

Bausch & Lomb Incorporated

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Propylene glycol (0.95%)

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
  • if single-use dispenser is not intact

When using this product

  • do not touch tip of container to any surface to avoid contamination
  • do not reuse
  • once applied, discard

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.

  • to open, completely twist off tab
  • squeeze 1 to 2 drops in the affected eye(s) as needed
  • throw away dispenser immediately after use. Do not reuse.
  • store at 15°-30°C (59°-86°F)
  • keep tightly closed
  • use before expiration date on dispenser

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

Advanced Eye Relief/ Dry Eye/ Rejuvenation Lubricant

Bausch & Lomb

ADVANCED Eye ReliefTM

Preservative-free

Dry Eye

Rejuvenation

LUBRICANT EYE DROPS

Fast relief from age-related dry eyes

Replenishes tears

Refreshes eyes

32 Sterile Single-Use Dispensers

0.02 FL OZ EA (0.6 mL EA)

Advanced Eye Relief/ Dry Eye/ Rejuvenation Lubricant

propylene glycol SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24208-453
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
propylene glycol Propylene Glycol 0.95 mL

Inactive Ingredients

Ingredient Name Strength
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 0.6 in 1 APPLICATOR
2 NDC:24208-453-32 32 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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