leader lubricating plus

Manufacturer
Cardinal Health
Effective date
2018-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:59:18

Label at a glance#

Productleader lubricating plus
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure13 sections

Indications and 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

Dosage and administration

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

Storage and handling

• store at 20-25 ° C (68-77 ° F) • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Label contents#

Full prescribing information#

Active ingredient (in each single-use container)

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose sodium 0.5%

Purpose

OTC - PURPOSE SECTION

Eye lubricant

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if solution changes color or becomes cloudy

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • store at 20-25°C (68-77°F)
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

1-800-719-9260

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sterile

Lubricating Plus

Carboxymethylcellulose Sodium 0.5%

Lubricant Eye Drops

Actual Size

COMPARE TO REFRESH PLUS®

active ingredient

100% Money Back Guarantee

Moisturizing Relief

Preservative Free

30 STERILE SINGLE-USE VIALS

0.01 FL OZ (0.4 mL) EACH

lubricating-plus-image
lubricating-plus-image

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70000-035270000-0352-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
06d0a353-17eb-47e5-9319-e8914e8fd7c2cdc419bf-c092-420f-874f-c3cc49071f212024-12-05WarningsExact identifier
spl set id: cdc419bf-c092-420f-874f-c3cc49071f21

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.