FDA.reportPublic FDA data

CorneaCare Recover for dry eyes

Manufacturer
CorneaCare Inc. | KC Pharmaceuticals, Inc. | Avizor, S.A.
Effective date
2023-12-23
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:17:15

Label at a glance#

ProductCorneaCare Recover for dry eyes
Active ingredientPOVIDONE, GLYCERIN
Label structure9 sections

Indications and uses

for temporary relief of burning and irritation due to dryness of the eye for temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun for use as a protectant against further irritation or to relieve dryness of the eye

Dosage and administration

remove tamper evident ring, then remove cap tip bottle at a downward angle or upside down (to deliver drop to eye) squeeze bottle to instill 1 or 2 drops in the affected eye(s) as needed replace cap after use

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Glycerin 0.63%

Povidone 0.25%

Purpose

OTC - PURPOSE SECTION

Lubricant

Lubricant

Uses

INDICATIONS & USAGE SECTION

  • for temporary relief of burning and irritation due to dryness of the eye
  • for temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
  • for use as a protectant against further irritation or to relieve dryness of the eye

Warnings

WARNINGS SECTION

For external use only

Do no use

OTC - DO NOT USE SECTION

  • if solution changes color or becomes cloudy
  • if tamper evident ring is broken or missing

When using this product

OTC - WHEN USING SECTION

  • do not touch tip of container to any surface to avoid contamination
  • replace cap after using

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you experience eye pain, changes in vision, continued redness or irritation of the eye
  • condition worsens or persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • remove tamper evident ring, then remove cap
  • tip bottle at a downward angle or upside down (to deliver drop to eye)
  • squeeze bottle to instill 1 or 2 drops in the affected eye(s) as needed
  • replace cap after use

Other information

OTHER SAFETY INFORMATION

store at 15°-30°C (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium hyaluronate

Questions or comments?

OTC - QUESTIONS SECTION

Call 267-217-3086 or email hello@mycorneacare.com or visit mycorneacare.com/artificial-tear

CorneaCare Recover for Dry Eyes 10mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CorneaCare Recover for Dry Eyes 10mLCorneaCare Recover for Dry Eyes 10mL

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
82875-00182875-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BORIC ACIDR57ZHV85D4IACT
MAGNESIUM CHLORIDE02F3473H9OIACT
SODIUM CHLORIDE451W47IQ8XIACT
POVIDONEFZ989GH94EACTIB
SODIUM BORATE91MBZ8H3QOIACT
GLYCERINPDC6A3C0OXACTIB
CALCIUM CHLORIDEM4I0D6VV5MIACT
POTASSIUM CHLORIDE660YQ98I10IACT
WATER059QF0KO0RIACT
HYALURONATE SODIUMYSE9PPT4THIACT

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
1fc31be8-8d8b-a7c7-e063-6294a90aabc0e3a731a9-ad76-3016-e053-2a95a90a4ec82024-08-15WarningsExact identifier
spl set id: e3a731a9-ad76-3016-e053-2a95a90a4ec8

Reported adverse events (FAERS/openFDA)#

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