Up & Up Lubricant Eye Drops 0.5 oz 2ct, Twin Pk NBE Refresh Tears 637 (2018)

Manufacturer
Target Corporation
Effective date
2018-04-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:59:37

Label at a glance#

ProductUp and Up Lubricant Refreshing Tears
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure12 sections

Storage and handling

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

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
  • replace cap after each use
  • 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 eyes 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

  • instill 1 or 2 drops in the affected eye(s) as needed

STORAGE AND HANDLING SECTION

Other information

  • store between 15-30°C (59-86°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium hydroxide

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Target Corporation

Minneapolis, MN 55403

Made in South Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

637637

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-63811673-638-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
c9de1091-0033-2cc5-e053-2a95a90a96626a4b70ee-74b8-2a06-e053-2991aa0a9a2f2021-08-18WarningsExact identifier
spl set id: 6a4b70ee-74b8-2a06-e053-2991aa0a9a2f

Reported adverse events (FAERS/openFDA)#

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