Dry Eye Therapy description, usages, side effects, indications, overdosage, supplying and lots more!

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Dry Eye Therapy

Western Family Foods Inc

Western Family Dry Eye Therapy Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Polyethylene glycol 400 0.4%

Propylene glycol 0.3%

Purpose

Lubricant

Dry Eye Therapy Uses

  • •for the temporary relief of burning and irritation due to dryness of the eye

Warnings

For external use only

Do not use

  • •if this product changes color or becomes cloudy

When using this product

  • •do not touch tip of container to any surface to avoid contamination
  • •do not reuse
  • •once opened, discard

Stop use and ask a doctor if

  • •you feel eye pain
  • •changes in vision occur
  • •redness or irritation of the eye(s) gets worse, persist or lasts more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

  • •instill 1 or 2 drops in the affected eye(s) as needed

Dry Eye Therapy Other information

  • •store at 20-25°C (68-77°F)

Inactive ingredients

boric acid, calcium chloride dihydrate, hypromellose, magnesium chloride hexahydrate, potassium chloride, sodium chloride, water for injection, zinc chloride. May contain sodium hydroxide and/or hydrochloric acid to adjust pH.

Package/Label Principal Display Panel

dry eye therapy

lubricant eye drops

long lasting relief

soothing comfort

Compare to the active ingredients of Systane® Lubricant Eye Drops

preservative-free vials

30 Sterile Single-Use Vials

0.01 FL OZ (0.4 mL) each

Dry Eye Therapy

Polyethylene glycol, Propylene glycol SOLUTION, GEL FORMING / DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55312-896
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
polyethylene glycol 400 Polyethylene Glycol 400 0.4 g
propylene glycol Propylene Glycol 0.3 g

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
calcium chloride
HYPROMELLOSES
MAGNESIUM CHLORIDE
potassium chloride
SODIUM CHLORIDE
water
ZINC CHLORIDE
SODIUM HYDROXIDE
HYDROCHLORIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.4 in 1 VIAL, SINGLE-DOSE
2 NDC:55312-896-65 30 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-11-25


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Be sure to consult your doctor before taking any medication!
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