CVS Redness Relief Maximum description, usages, side effects, indications, overdosage, supplying and lots more!

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CVS Redness Relief Maximum

CVS PHARMACY, INC.




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients                                     Purpose

Dextran 70 0.1%.................................... Lubricant

Polyethylene glycol 400 1%..................... Lubricant

Povidone 1%.......................................... Lubricant

Tetrahydrozoline HCI 0.05%..................... Redness Reliever

Purpose

Uses

  • for the relief of redness of th eyes 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 becomes cloudy
  • to avoid contamination, do not touch tip of container to any surface

Stop use and ask a doctor if

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

If pregnant or breast-feeding, ask a health professional before use

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

Uses

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

Other information

  • some users may experience a brief tingling sensation
  • store at 15° to 25°C (59° to 77°F)

Inactive ingredients:

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate, sodium chloride

DISTRIBUTED BY:

CVS PHARMACY, INC.

ONE CVS DRIVE

WOONSOCKET, RI 02895 USA

CVS Redness Relief Maximum

CVS Redness Relief Maximum

Dextran 70 Polyethylene glycol 400 Povidone Tetrahydrozoline HCI SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-731
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTRAN 70 DEXTRAN 70 .001 mg
polyethylene glycol 400 Polyethylene Glycol 400 .01 mg
povidone .01 mg
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE .0005 mg

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:59779-731-15 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2014-03-06


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Be sure to consult your doctor before taking any medication!
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