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

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Visine A.C.

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

Visine A.C.® Eye Drops


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Tetrahydrozoline HCl 0.05% Redness reliever
Zinc sulfate 0.25% Astringent

Use

  • for temporary relief of discomfort and 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 A.C. 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 chloride, sodium citrate

Questions?

call 1-888-734-7648

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

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton

Sterile
Visine®
A.C.®
ASTRINGENT / REDNESS
RELIEVER EYE DROPS
Seasonal Itching +
Redness Relief

Relieves
itching,
burning,
watery eyes
due to
pollen, dust,
ragweed

1 FL OZ (30mL)

Visine A.C.

Visine A.C.

Tetrahydrozoline Hydrochloride and Zinc Sulfate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-201
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE 0.5 mg
ZINC SULFATE 2.5 mg

Inactive Ingredients

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

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:42002-201-35 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-09-16


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Be sure to consult your doctor before taking any medication!
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