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

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Redness Relief Original

CVS Pharmacy
Bausch & Lomb Incorporated

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Naphazoline hydrochloride (0.012%)

Polyethylene glycol 300 (0.2%)

Purpose

Redness reliever

Lubricant

Redness Relief Original Uses

  • relieves redness of the eye due to minor eye irritations
  • temporary relief of burning and irritation due to dryness of the eye
  • protects against further irritation

Warnings

Do not use

  • if solution changes color or becomes cloudy

Ask a doctor before use if you have

  • narrow angle glaucoma

When using this product

  • do not touch tip of container to any surface to avoid contamination
  • do not overuse as it may produce increased redness of the eye
  • pupils may become enlarged temporarily
  • 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.

Directions

  • instill 1 to 2 drops in the affected eye(s) up to four times daily

Redness Relief Original Other information

  • store at 15°-30°C (59°-86°F)
  • keep tightly closed
  • use before expiration date marked on the carton and bottle
  • serious side effects associated with use of the product may be reported to the phone number provided below

Inactive ingredients

benzalkonium chloride (0.01%), boric acid, edetate disodium, sodium borate, sodium chloride

Questions ?

Call: 1-866-767-9161

Package/Label Principal Display Panel

Redness Relief Original

CVS pharmacy

CVS Pharmacist Recommended

REDNESS RELIEF ORIGINAL

Redness Reliever/Lubricant Eye Drops

Fast acting formula

0.5 FL OZ (15 mL)

Redness Relief Original

Naphazoline Hydrochloride and Polyethylene glycol 300 SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-219
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
naphazoline hydrochloride Naphazoline 0.1 mg
POLYETHYLENE GLYCOL 300 2 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
BORATE ION
SODIUM BORATE
SODIUM CHLORIDE
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:59779-219-20 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-09-13


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Be sure to consult your doctor before taking any medication!
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