Octiq Sodium Chloride Eye Ointment

Manufacturer
Innovus Pharmaceuticals, Inc. | AMMAN PHARMACEUTICAL INDUSTRIES
Effective date
2023-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:40:27

Label at a glance#

ProductOctiq
Active ingredientSODIUM CHLORIDE
Label structure13 sections

Dosage and administration

pull down lower lid of the affected eye(s) and apply a small amount (1/4 inch) to the inside of the eyelid  apply every 3 - 4 hours, or as directed by a doctor.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride 5%

Purpose

OTC - PURPOSE SECTION

Hypertonicity agent

Use

INDICATIONS & USAGE SECTION

For the temporary relief of corneal edema

Warnings

WARNINGS SECTION

  • For use in the eyes only
  • Retain outer carton for full product drug facts

Do not use 

OTC - DO NOT USE SECTION

this product except under the advice and supervision of a doctor

When using this product

OTC - WHEN USING SECTION

  • To avoid contamination, do not touch tip of container to any surface
  • Replace cap after use
  • This product may cause temporary burning and irritation on being instilled into the eye

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • pull down lower lid of the affected eye(s) and apply a small amount (1/4 inch) to the inside of the eyelid 
  • apply every 3 - 4 hours, or as directed by a doctor.

Other Information 

OTHER SAFETY INFORMATION

  • Store at room temperature 15°C-30°C (59°F-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Lanolin alcohol, Methyl paraben, Paraffin oil, Propyl paraben, Propylene glycol, Purified water, White Petrolatum

Questions or commetns?

OTC - QUESTIONS SECTION

Call 1.800.996.5122  (Mon-Fri 9AM-5PM EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57483-60157483-601-05

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
875ca176-e8b4-45ae-9d27-e329b0f860c661fffceb-7f35-45a7-a7b7-c3b31c240fbc2023-07-12WarningsExact identifier
spl set id: 61fffceb-7f35-45a7-a7b7-c3b31c240fbc

Reported adverse events (FAERS/openFDA)#

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