i-Drops ARTIFICIAL TEARS

Manufacturer
GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Effective date
2021-03-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:48:03

Label at a glance#

Producti-Drops ARTIFICIAL TEARS
Active ingredientHYPROMELLOSE, UNSPECIFIED, NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80, ZINC SULFATE, UNSPECIFIED FORM
Label structure10 sections

Indications and uses

• For use as a protectant against further irritation or to relieve dryness of the eye. • For the temporary relief of burning & irritation due to the dryness of the eye. • Relieves redness of the eye due to minor eye irritations.

Dosage and administration

Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Storage and handling

• Store at room temperature. • Remove contact lenses before using. • Tamper Evident:  Do not use if neckband on bottle is broken or missing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Hypromellose 0.20%
Naphazoline Hydrochloride 0.025%
Polysorbate 80 0.50%
Zinc Sulfate 0.25%

PURPOSE

OTC - PURPOSE SECTION

Lubricant
Redness Reliever
Lubricant
Lubricant

Uses

INDICATIONS & USAGE SECTION

• For use as a protectant against further irritation or to relieve dryness of the eye.

• For the temporary relief of burning & irritation due to the dryness of the eye.

• Relieves redness of the eye due to minor eye irritations.

Warnings

WARNINGS SECTION

For external use only.

Do not use if solution changes color or becomes cloudy.

Ask a doctor before use if you have narrow angle glaucoma

When using this product: • To avoid contamination, do not touch tip of container to any surface. • Replace cap after using. • Overuse of this product may produce increased redness of the eye. • Pupils may become enlarged temporarily.

Stop use and ask a doctor if
• You experience eye pain
• You experience changes in vision
• You experience continued redness or irritation of the eye
• The condition worsens
• Symptoms last 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Other information

STORAGE AND HANDLING SECTION

• Store at room temperature.

• Remove contact lenses before using.

• Tamper Evident: Do not use if neckband on bottle is broken or missing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Calcium chloride, Citric acid, Edetate disodium, Magnesium chloride, Potassium chloride, Purified water, Sodium citrate, Sodium chloride and Sorbic acid.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-572-6632, weekdays, 7:00 AM - 5:30 PM EST.

SPL UNCLASSIFIED SECTION

Relieve dryness of the eye

Manufactured by :

Global Pharma Healthcare Pvt. Ltd.,

A-9, SIDCO Pharmaceutical Complex,

Alathur-603 110 - INDIA.

www.global-pharma.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Eye09Eye09

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73921-009-152023-02-08C16284748780-1f386c649-f531-0266-e053-dadaa90a7c1ai-Drops ARTIFICIAL TEARS
73921-009-152023-01-30C16284748780-1f386c649-f531-0266-e053-dadaa90a7c1ai-Drops ARTIFICIAL TEARS

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73921-00973921-009-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
f42b5aca-6d90-2a78-e053-2a95a90a342a03ae5fee-1901-44e5-b0b2-3c4311e44db12023-02-08WarningsExact identifier
spl set id: 03ae5fee-1901-44e5-b0b2-3c4311e44db1

Reported adverse events (FAERS/openFDA)#

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