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Visine

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

Visine Tired Eye Relief


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Glycerin 0.2% Lubricant
Hypromellose 0.36% Lubricant
Polyethylene glycol 400 1% Lubricant

Visine Uses

  • for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun
  • for protection against further irritation

Warnings

When using this product

  • 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 or 2 drops in the affected eye(s) as needed
  • children under 6 years of age: ask a doctor

Visine Other information

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

Inactive ingredients

ascorbic acid, benzalkonium chloride, boric acid, dextrose, glycine, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium citrate, sodium lactate, sodium phosphate dibasic

Questions?

Call 1-888-734-7648

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

PRINCIPAL DISPLAY PANEL - 15mL Bottle Carton

Sterile
Visine®
TIRED EYE
Relief
LUBRICANT EYE DROPS

UP
TO
10
HOURS COMFORT
HYDROBLEND®

Soothes +
revives tired,
overworked
eyes
with HYDROBLEND®
moisturizers
for up to 10 hours
of comfort

1/2 FL OZ (15mL)

Visine

Visine

Glycerin, Hypromelloses, and Polyethylene Glycol 400 SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-212
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GLYCERIN 2.5 mg
HYPROMELLOSES 3.6 mg
polyethylene glycol 400 Polyethylene Glycol 400 11.28 mg

Inactive Ingredients

Ingredient Name Strength
ASCORBIC ACID
benzalkonium chloride
BORIC ACID
DEXTROSE
glycine
MAGNESIUM CHLORIDE
potassium chloride
water
SODIUM BORATE
SODIUM CHLORIDE
SODIUM CITRATE
sodium lactate
SODIUM PHOSPHATE, DIBASIC

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, PLASTIC
2 NDC:42002-212-15 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2012-05-18


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Be sure to consult your doctor before taking any medication!
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