NBE Refresh Optive Single Eye Drops 0.4 ml 13548ZZ (2018)

Manufacturer
United Exchange Corp.
Effective date
2018-01-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:04:18

Label at a glance#

ProductRefresh Optive Single Vial
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN
Label structure10 sections

Storage and handling

Other information use only if single-use container is intact use before expiration date marked on the container store at 59°-86°F (15°-30°C)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Carboxymethylcellulose sodium 0.5%................Eye Lubricant

Glycerin 0.9%......................................................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 irritaiton

WARNINGS SECTION

Warnings

  • for external use only
  • to avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
  • Do not touch tip unit-dose to eye
  • If solution changes color, 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 the eye, or if 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 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.

If used for post-operative (e.g. LASIK) dryness and discomfort, follow your eye doctor's instructions

STORAGE AND HANDLING SECTION

Other information

  • use only if single-use container is intact
  • use before expiration date marked on the container
  • store at 59°-86°F (15°-30°C)

INACTIVE INGREDIENT SECTION

Inactive ingredients

boric acid, calcium chloride, levocarnitine, magnesium chloride, polyethylene glycol 400, potassium chloride, purified water, sodium borate, trisodium citrate dihydrate

DOSAGE & ADMINISTRATION SECTION

Made in South Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

single.1single.1

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65923-54865923-548-04

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 · Source PDF

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
d0654976-ad6d-7121-e053-2a95a90a3bae638ad65c-4ce0-2aa0-e053-2991aa0a01c42021-11-09WarningsExact identifier
spl set id: 638ad65c-4ce0-2aa0-e053-2991aa0a01c4

Reported adverse events (FAERS/openFDA)#

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