Optase

Manufacturer
Scope Health Inc
Effective date
2026-01-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:35:45

Label at a glance#

ProductOptase
Active ingredientGLYCERIN
Label structure10 sections

Label contents#

Full prescribing information#

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.

OTC - ACTIVE INGREDIENT SECTION

0.3 % glycerin

OTC - PURPOSE SECTION

Eye Lubricant

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Borax, Boric Acid, Citric Acid anhydrous,
Sodium Chloride, Sodium Citrate Dihydrate, Sodium Hyaluronate, water.

DOSAGE & ADMINISTRATION SECTION

Directions:
Put one or two drops in the
affected eyes as needed.

WARNINGS SECTION

Warning
■ For external use only.
■ If solution changes color or becomes cloudy, do not use.
■ To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
Stop use and ask doctor if
■ You feel eye pain.
■ Changes in vision occur.
■ Redness or irritation of the eye lasts.
■ Condition worsens or lasts more than 72 hours.

INDICATIONS & USAGE SECTION

Uses
• For use as a lubricant to prevent
further irritation.
• May be used as a protectant against
further irritation.
• To relieve dryness of the eye.

Immediate Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Immediate LabelImmediate Label

Optase Hylo - Full Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Optase Hylo Forte Outer BoxOptase Hylo Forte Outer Box

Sample Box - Not for resale

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Optase Hylo Forte Sample BoxOptase Hylo Forte Sample Box

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860010859117GTIN-13: 0860010859117
EAN-13: 0860010859117
GTIN-12: 860010859117
UPC-A: 860010859117
GTIN storage (14 digits): 00860010859117
OPTASE HYLO FORTE box 2025 (P) V2- resize.jpg, OPTASE HYLO FORTE SAMPLE box 2025 (P) V2- resize.jpg
QR code linkQR Codeoptase.com/how-to-get-the-best-results/OPTASE HYLO FORTE box 2025 (P) V2- resize.jpg, OPTASE HYLO FORTE SAMPLE box 2025 (P) V2- resize.jpg
QR code linkQR Codeoptase.com/hylo-forte/OPTASE HYLO FORTE box 2025 (P) V2- resize.jpg, OPTASE HYLO FORTE SAMPLE box 2025 (P) V2- resize.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72972-008-01Optase1 in 1 BOXSOLUTION/ DROPS12
72972-008-01Optase10 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS102

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72972-00872972-008-01

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
OptaseGLYCERINScope Health Inc376e0289-28e9-e87f-e063-6294a90a3b042026-01-30WarningsExact identifier
ndc (package): 72972-008-01
ndc (product): 72972-008
ndc11 (package): 72972000801
spl id: 49961a0b-9956-de48-e063-6394a90a7c53
spl set id: 376e0289-28e9-e87f-e063-6294a90a3b04

Reported adverse events (FAERS/openFDA)#

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