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

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Visine

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

Visine L.R.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Oxymetazoline HCl 0.025%

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

  • 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

  • adults and children 6 years of age and over: put 1 or 2 drops in the affected eye(s)
  • this may be repeated as needed every 6 hours or as directed by a doctor
  • children under 6 years of age: ask a doctor

Visine Other information

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

Inactive ingredients

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

Questions?

call 1-888-734-7648, weekdays

PRINCIPAL DISPLAY PANEL - 15 mL Carton

LONG-
LASTING
REDNESS
RELIEF

Sterile
Visine ®
L.R. ®

LONG-LASTING
REDNESS RELIEF

OXYMETAZOLINE HCl
REDNESS RELIEVER EYE DROPS

  • Gets The Red Out ®
  • Up To 6 Hours Relief

1/2 FL OZ(15 mL)

Visine

Visine

Oxymetazoline Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-204
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OXYMETAZOLINE HYDROCHLORIDE OXYMETAZOLINE 0.25 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, PLASTIC
2 20 in 1 BOTTLE, PLASTIC
3 30 in 1 BOTTLE, PLASTIC
4 NDC:42002-204-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019407 2010-04-05


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