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.

VisineSummer Spectrum Relief


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Dextran 70 0.1% Lubricant
Polyethylene glycol 400 1% Lubricant
Povidone 1% Lubricant
Tetrahydrozoline HCl 0.05% Redness reliever

Uses

  • 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 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

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 1-800-223-0182, weekdays, 9 AM – 5 PM EST

PRINCIPAL DISPLAY PANEL - 15 mL Carton

Sterile
Visine
®

SUMMER
Spectrum Relief

LUBRICANT / REDNESS
RELIEVER EYE DROPS

Relieves
eye irritation
caused by
swimming,
sun or wind

Moisturizes
to protect against
further irritation

1/2 FL OZ (15mL)

Visine

Visine

Tetrahydrozoline Hydrochloride, Polyethylene Glycol 400, Povidone, and Dextran 70 LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-213
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE 0.5 mg
polyethylene glycol 400 Polyethylene Glycol 400 11.28 mg
povidone 10 mg
DEXTRAN 70 DEXTRAN 70 1 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:42002-213-05 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-01-01


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Be sure to consult your doctor before taking any medication!
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