Topcare Lubricating Plus description, usages, side effects, indications, overdosage, supplying and lots more!

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Topcare Lubricating Plus

Topco Associates LLC

Topco Associates LLC. Lubricating Plus Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Topcare Lubricating Plus Uses

  • •for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun
  • •may be used as a protectant against further irritation

Warnings

For external use only

Do not use

if solution changes color or becomes cloudy

When using this product

to avoid contamination

  • •do not touch tip of container to any surface
  • •do not reuse
  • •once opened, discard
  • •do not touch unit-dose tip to eye

Stop use and ask a doctor if

  • •you experience eye pain
  • •changes in vision occur
  • •redness or irritation of the eye continues
  • •redness or irritation of the eye worsens or persists for 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

  • •to open, twist and pull tab to remove
  • •instill 1 or 2 drops in the affected eye(s) as needed and discard container

Topcare Lubricating Plus Other information

  • •store at 20-25oC (68-77oF)
  • •RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive Ingredients

calcium chloride dihydrate, magnesium chloride hexahydrate, potassium chloride, sodium chloride, sodium lactate solution, water for injection. May also contain sodium hydroxide and/or hydrochloric acid to adjust pH.

Questions or comments?

1-888-423-0139

Package/Label Principal Display Panel

SENSITIVE PRESERVATIVE FREE

Lubricating Plus

Lubricant Eye Drops

CARBOXYMETHYLCELLULOSE SODIUM 0.5%

Moisture drops for dry eyes

COMPARE TO Refresh Plus® active ingredient

70 SINGLE-USE CONTAINERS

0.01 FL OZ (0.4 mL) EACH STERILE

Topcare Lubricating Plus

carboxymethylcellulose sodium SOLUTION, GEL FORMING / DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:36800-323
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 0.5 g

Inactive Ingredients

Ingredient Name Strength
calcium chloride
MAGNESIUM CHLORIDE
potassium chloride
SODIUM CHLORIDE
sodium lactate
water
SODIUM HYDROXIDE
HYDROCHLORIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.4 in 1 VIAL, SINGLE-USE
2 0.4 in 1 VIAL, SINGLE-USE
3 NDC:36800-323-65 30 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-08-20


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