Up & Up Preservative Free Eye Drops 70 ct. NBE Refresh Plus 636 (2018)

Manufacturer
Target Corporation
Effective date
2018-04-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:15

Label at a glance#

ProductUp and Up Lubricant Refreshing
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure12 sections

Storage and handling

Other information store between 15-30°C (59-86°F) protect from light

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, 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 SECTION

Warnings

For external use only

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
  • do not use if this solution changes color or becomes cloudy
  • remove contact lenses before using

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • continued redness or irritation of the eye lasts
  • condition worsens or lasts more than 72 hours

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

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
  • children under 6 years of age: ask a doctor

STORAGE AND HANDLING SECTION

Other information

  • store between 15-30°C (59-86°F)
  • protect from light

INACTIVE INGREDIENT SECTION

Inactive ingredients calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide, sodium lactate

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Target Corporation

Minneapolis, MN 55403

Made in South Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

636636

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionPSN1
1188426carboxymethylcellulose sodium 5 MG/ML Ophthalmic SolutionSCD1
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionSY1
1188426carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
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1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
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9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
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cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
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87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-636-702024-01-30C16284748780-11030e365-5bca-111a-e063-dadaa90a10e2Up & Up Preservative Free Eye Drops 70 ct. NBE Refresh Plus 636 (2018)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-636-70Up and Up Lubricant Refreshing70 in 1 CARTONSOLUTION/ DROPS701
11673-636-70Up and Up Lubricant Refreshing0.4 mL in 1 VIALSOLUTION/ DROPS0.41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-636UP AND UP LUBRICANT REFRESHING (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [TARGET CORPORATION]1Legacy NDC, 2 package rows20180421_6a3d8a45-5506-1504-e053-2a91aa0ab133.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-63611673-636-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
6a3d8a45-5507-1504-e053-2a91aa0ab1336a3d8a45-5506-1504-e053-2a91aa0ab1332018-04-19WarningsExact identifier
spl id: 6a3d8a45-5507-1504-e053-2a91aa0ab133
spl set id: 6a3d8a45-5506-1504-e053-2a91aa0ab133

Reported adverse events (FAERS/openFDA)#

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