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

CareOne Lubricant

American Sales Company

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
American Sales Company Lubricant Eye Drops Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Polyethylene glycol 400 0.4%

Propylene glycol 0.3%

Purpose

Lubricant

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

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.

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Compare to the Active Ingredients in Systane® Lubricant Eye Drops

LUBRICANT EYE DROPS

Polyethylene Glycol 400 0.4%

Propylene Glycol 0.3%

PRESERVATIVE FREE VIALS

Long Lasting Relief

Soothing Comfort

Dry Eye Therapy

30 Sterile Vials

0.01 FL OZ

(0.4 mL) Each

CareOne Lubricant

Polyethylene glycol, Propylene glycol SOLUTION, GEL FORMING / DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41520-896
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 0.04 in 1 VIAL
2 NDC:41520-896-65 30 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-07-09


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Be sure to consult your doctor before taking any medication!
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