Rugby 47692 47693 Carboxymethylcellulose 0.5% Ophthalmic Solution 0.4mL

Manufacturer
Rugby Laboratories
Effective date
2026-06-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
weekly-update
Hydrated at
2026-07-17 21:43:28

Label at a glance#

ProductLubricant Eye
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
Label structure12 sections

Storage and handling

Other information  Use only if tamper seal on top and bottom flaps are intact.  Store between 15-30°C (59-86°F).  Keep carton for complete product information.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose
Carboxymethylcellulose sodium (0.5%)...............................................................Eye lubricant

OTC - PURPOSE SECTION

Uses
 For the temporary relief of burning and irritation due to dryness of the eye.
 For the temporary relief of discomfort due to minor irritations of the eye or from exposure
to wind or sun.
 For use as a lubricant to prevent further irritation or to relieve dryness of the eye.

WARNINGS SECTION

Warnings
For use in the eyes only.

OTC - DO NOT USE SECTION

Do not use if solution changes color or becomes cloudy.

OTC - WHEN USING SECTION

When using this product
 do not touch tip of container to any surface to avoid contamination.
 do not reuse; once opened discard.

OTC - STOP USE SECTION

Stop use and ask a doctor if
 you experience eye pain, changes in vision, continued redness or irritation of the eye.
 the condition worsens or persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Directions
 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 SECTION

Other information
 Use only if tamper seal on top and bottom flaps are intact.
 Store between 15-30°C (59-86°F).  Keep carton for complete product information.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride,
sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

DOSAGE & ADMINISTRATION SECTION

Rugby 30 pcsRugby 30 pcsQuestions or comments?
Call 1-888-645-8204 MONDAY-FRIDAY 9AM-5PM (PST)

*This product is not manufactured or distributed by Allergan, Inc., an AbbVie company, distributor of
Refresh Plus® Preservative-Free Lubricant Eye Drops.

Distributed by:

RUGBY LABORATORIES

Indianapolis, IN 46268

(800) 616-2471

www.major-rugby.com

Rev. 12/25 R-110 Re-order No. 371267

Rev. 12/25 R-110 Re-order No. 371268

Made in U.S.A.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 Vial Rugby50 Vial RugbyRugby 50 pcsRugby 50 pcs30 Vial Rugby30 Vial Rugby

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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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
0536-14760536-1476-92, 0536-1476-93

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-05-14full-release2026-06-01 01:57:31

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
Lubricant EyeCARBOXYMETHYLCELLULOSE SODIUMRugby Laboratories51cadca6-a31b-c1b5-e063-6394a90a34d32026-06-15WarningsExact identifier
ndc (package): 0536-1476-93
ndc (package): 0536-1476-92
ndc (product): 0536-1476
ndc11 (package): 00536147692
ndc11 (package): 00536147693
spl id: 5452d0c5-f378-52eb-e063-6394a90a7d85
spl set id: 51cadca6-a31b-c1b5-e063-6394a90a34d3

Reported adverse events (FAERS/openFDA)#

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