CVS Pharmacy, Inc. Lubricant Eye Drops Drug Facts

Manufacturer
CVS Pharmacy
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:09:48

Label at a glance#

Productlubricant eye
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
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

Compare to the active ingredient in Refresh Plus®

Preservative Free

Lubricant Eye Drops

CARBOXYMETHYLCELLULOSE SODIUM 0.5%

For sensitive eyes

Instantly moisturizes & relieves dry, irritated eyes

Long lasting relief plus protection

Actual Product Size on Side Panel

70 STERILE SINGLE-USE CONTAINERS

0.01 FL OZ (0.4 mL) EACH

lubricant-eye-drops-imagelubricant-eye-drops-image

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69842-739-01EA - Each69842-73929912abc-bf9f-41be-92d3-2993b4c6950812019-06-19

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-73969842-739-01, 69842-739-65

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
13bfe686-bcc4-4e1f-8e47-23b05605a46b3f9ab963-0bfb-4eb4-bda4-985dd6ca39022020-10-26WarningsExact identifier
spl id: 13bfe686-bcc4-4e1f-8e47-23b05605a46b
spl set id: 3f9ab963-0bfb-4eb4-bda4-985dd6ca3902

Reported adverse events (FAERS/openFDA)#

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