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

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Visine Original

Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.

Visine Original Redness Relief Eye Drops


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Tetrahydrozoline HCl 0.05%

Purpose

Redness reliever

Use

  • for the relief of redness of the eye due to minor eye irritations

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
  • 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

Visine Original Other information

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

Inactive ingredients

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

Questions?

call 1-888-734-7648

Dist: Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc., Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton

Sterile
Visine ®

ORIGINAL
Redness Relief
TETRAHYDROZOLINE HCl
REDNESS RELIEVER EYE DROPS

Gets the
Red Out
®

Fast-acting
formula

1/2 FL OZ (15mL)

Visine Original

Visine Original

Tetrahydrozoline Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-203
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE 0.5 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
2 30 in 1 BOTTLE
3 19 in 1 BOTTLE
4 NDC:42002-203-35 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-08-25


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