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Advanced relief

Kareway Product, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Dextran 70 0.1%

Polyethylene Glycol 400 1%

Povidone 1%

Tetrahydrozoline HCl 0.5%

Purpose

Lubricant

Lubricant

Lubricant

Redness reliever

Use

  • for the relief of redness of the eye due to minor eye irritations
  • for use as a protectant against further irritation or to relieve dryness of the eye

Warnings

Ask a doctor before use if you have narrow angle glaucoma

When using this product

  • pupils may become enlarged temporarily
  • overuse may cause more eye redness
  • remove contact lenses before using
  • do not use if this solution changes color or become cloudy
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts
  • condition worsens or lasts more than 72 hours

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

  • Put 1 to 2 drops in the affected eye(s) up to 4 times daily
  • children under 6 years of age:  ask a doctor

Advanced relief Other information

  • store between 15 ° to 25 ° C (59 ° F to 77 ° F)


Inactive ingredients

boric acid, sodium borate, edetate disodium, benzalkonium chloride, sodium chloride, dilite hydrochloric acid, sterile purified water

package label

Advance reliefAdvanced relief

Advanced relief

dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline HCl LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67510-0064
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE 0.5 mg
DEXTRAN 70 DEXTRAN 70 1 mg
polyethylene glycol 400 Polyethylene Glycol 400 10 mg
povidone 10 mg

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:67510-0064-5 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-08-11


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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