Optiq Balance

Manufacturer
Optiq Eyecare LLC
Effective date
2025-09-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:38:25

Label at a glance#

ProductOptiq Restore
Active ingredientLIGHT MINERAL OIL, MINERAL OIL
Label structure8 sections

Indications and uses

Temporary relief of burning and irritation due to dryness of the eye Temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun As a protectant to prevent further irritation or to relieve dryness of the eye

Dosage and administration

Shake well before use Instill 1 to 2 drop(s) in the affected eye(s) as needed or as directed by your doctor See side of carton for directions for use

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts

Active IngredientsPurpose
Light mineral oil (0.6%)Emollient
Mineral oil (0.6%)Emollient

OTC - PURPOSE SECTION

Uses

INDICATIONS & USAGE SECTION

  • Temporary relief of burning and irritation due to dryness of the eye
  • Temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
  • As a protectant to prevent further irritation or to relieve dryness of the eye

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if emulsion changes color
  • if you are sensitive to any ingredient in this product

When using this product

OTC - WHEN USING SECTION

  • Do not touch the tip of container to any surface to avoid contamination
  • Replace cap after each use

OTC - STOP USE SECTION

Stop use and ask a doctor ifyou experience any of the following:

  • Eye pain
  • Changes in vision
  • Continued redness or irritation of the eye
  • 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Shake well before use
  • Instill 1 to 2 drop(s) in the affected eye(s) as needed or as directed by your doctor
  • See side of carton for directions for use

Other Information

SPL UNCLASSIFIED SECTION

  • Temporarily blurred vision is typical upon application
  • Drops appear as a milky white emulsion
  • Store at 15-25°C (59-77°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Gellan Gum, Glyceryl Monostearate, Polysorbate 80, Hypromellose, Sodium Hyaluronate, Trehalose, Mannitol, Tromethamine and Purified Water.

Questions?

OTC - QUESTIONS SECTION

Call: 1-877-696-7848

hello@optiqeyecare.com
www.optiqeyecare.com

Directions for Use:

1. Hold the bottle just below the cap and twist the cap to open.
2. Before first use, hold the bottle upside down and dispense one drop of product to discard.
3. Shake the bottle downward to remove residual product (see picture).

Use diagramUse diagram

4. Place 1 or 2 drops as needed in the affected eye(s) and blink.
5. After use, shake the bottle downward to remove residual product that may be left on the tip (picture above).
6. Replace cap after use.

Tamper Evident

For your protection this bottle has a tamper evident ring around the bottom of the cap. Do not use if this ring is damaged or missing at the time of purchase. 

Marketed and Distributed by:
Optiq Eyecare
PO Box 32
Paramus, NJ 07652

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Optiq Eyecare

NDC: 85949-113-10

Optiq

RESTORE

ADVANCED LIPID COMPLEX

MGD RELIEF

Carton labelCarton label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130385949113104GTIN-13: 0385949113104
EAN-13: 0385949113104
GTIN-12: 385949113104
UPC-A: 385949113104
GTIN storage (14 digits): 00385949113104
Optiq Restore.jpg
QR code linkQR Codeen.m.wikipedia.org/Optiq Restore.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85949-11385949-113-10

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-09-20full-release2026-06-01 01:14:30

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
51266787-b513-bc15-e063-6394a90ad16fe9fbc4b5-716a-4caa-9bab-b4a4981811142026-05-06WarningsExact identifier
spl set id: e9fbc4b5-716a-4caa-9bab-b4a498181114

Reported adverse events (FAERS/openFDA)#

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