FDA.reportPublic FDA data

Octiq Lubricant Eye Drops

Manufacturer
Innovus Pharmaceuticals, Inc. | AMMAN PHARMACEUTICAL INDUSTRIES
Effective date
2024-07-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:58:34

Label at a glance#

ProductOctiq Lubricant Eye Drops
Active ingredientDEXTRAN 70, HYPROMELLOSE 2910 (4000 MPA.S)
Label structure13 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Dextran 70 0.1%

Hypromellose 2910 0.3%

Purpose

OTC - PURPOSE SECTION

Lubricant

Lubricant

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if solution changes color or becomes cloudy
  • if you are sensitive to any ingredient in this product

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you feel eye pain
  • changes in vision occur redness or irritation of the eye gets worse or lasts 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information 

OTHER SAFETY INFORMATION

  • Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Boric acid, disodium edetate, potassium chloride, povidone, purified water, sodium borate, sodium chloride
Preservative added: benzalkonium choride

Questions?

OTC - QUESTIONS SECTION

Call 1.800.996.5122

(Mon-Fri 9AM-5PM EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
57483-61057483-610-15

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
DEXTRAN 707SA290YK68ACTIB
HYPROMELLOSE 2910 (4000 MPA.S)RN3152OP35ACTIB
BORIC ACIDR57ZHV85D4IACT
EDETATE DISODIUM7FLD91C86KIACT
POTASSIUM CHLORIDE660YQ98I10IACT
POVIDONEFZ989GH94EIACT
WATER059QF0KO0RIACT
SODIUM BORATE91MBZ8H3QOIACT
SODIUM CHLORIDE451W47IQ8XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT

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
2a98ec01-c50f-45c1-83c1-fdbd3e3d53f6407eeffb-cb32-44bc-aef4-b1b654ac61592024-07-20WarningsExact identifier
spl id: 2a98ec01-c50f-45c1-83c1-fdbd3e3d53f6
spl set id: 407eeffb-cb32-44bc-aef4-b1b654ac6159

Reported adverse events (FAERS/openFDA)#

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