EYE DROPS

Manufacturer
Foshan Sugar Max Cosmetics CO.,Ltd
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:29:36

Label at a glance#

ProductEYE DROPS
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Label structure11 sections

Storage and handling

Use only if tape seals on top and bottom flaps areintact. Use before expiration date marked on container. Discard 90 days after opening.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

EYE DROPS

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose sodium 0.25%

OTC - PURPOSE SECTION

Eye lubricant

INDICATIONS & USAGE SECTION

Uses For the temporary relief of burning, irritation, anddiscomfort due to dryness of the eye or exposure towind or sun.
May be used as a protectant against further irritation.

WARNINGS SECTION

For external use only.
To avoid contamination, do not touch tip of container toany surface. Replace cap after using.
lf solution changes color or becomes cloudy, do not use.

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience eye pain,changes in vision, continued redness or irritation of theeye, or if the condition worsens or persists for more than72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medicalhelp or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions Instilllor 2 drops in the affected eye(s) asneeded

STORAGE AND HANDLING SECTION

Use only if tape seals on top and bottom flaps areintact.
Use before expiration date marked on container.
Discard 90 days after opening.

INACTIVE INGREDIENT SECTION

calciumchloride
Dequest
magnesium chloride
potassium chloride
purified water
sodium bicarbonate
sodium chloride
sodium perborate
sodium phosphate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1547948carboxymethylcellulose sodium 0.25 % Ophthalmic SolutionPSN3
1547948carboxymethylcellulose sodium 2.5 MG/ML Ophthalmic SolutionSCD3
1547948carboxymethylcellulose sodium 0.25 % Ophthalmic SolutionSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130198715575279GTIN-13: 0198715575279
EAN-13: 0198715575279
GTIN-12: 198715575279
UPC-A: 198715575279
GTIN storage (14 digits): 00198715575279
label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
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cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
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362d7abb-94e6-4c60-9a58-266894157713Product name120231023
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9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
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0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
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7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
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8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-001-01EYE DROPS15 mL in 1 BOTTLELIQUID153
84938-001-01EYE DROPS2 in 1 BOXLIQUID23

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84938-00184938-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
EYE DROPSCARBOXYMETHYLCELLULOSE SODIUMFoshan Sugar Max Cosmetics CO.,Ltd26dbf100-593e-3778-e063-6394a90adf262025-12-30WarningsExact identifier
ndc (package): 84938-001-01
ndc (product): 84938-001
ndc11 (package): 84938000101
spl id: 47373d02-07ae-7104-e063-6294a90a0265
spl set id: 26dbf100-593e-3778-e063-6394a90adf26

Reported adverse events (FAERS/openFDA)#

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