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 22:48:05

Label at a glance#

Producti-Drops ARTIFICIAL TEARS
Active ingredientPOLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE, UNSPECIFIED
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 discomfort due to minor irritations of the eye, or to exposure to wind or sun

Dosage and administration

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

Storage and handling

Store at 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Polyvinyl alcohol 0.5%

Povidone 0.6%

PURPOSE

OTC - PURPOSE SECTION

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 discomfort due to minor irritations of the eye, or to exposure to wind or sun

Warnings

WARNINGS SECTION

For external use only.

Do not use this product if 

• Solution changes color or becomes cloudy

When using this product
• Remove contact lens before using
• To avoid contamination, do not touch tip of container to any surface
• Replace cap after using. Keep container tightly closed.

Stop use and ask a doctor if you experience
•  Eye pain, • Changes in vision,
• Continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.
If accidentally swallowed, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

Store at 15°-30°C (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium chloride, Dextrose, Edetate disodium, Potassium chloride, Purified water, Sodium bicarbonate, Sodium chloride, Sodium citrate, Sodium phosphate dibasic, Sodium phosphate monobasic.

Questions?

OTC - QUESTIONS SECTION

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

SPL UNCLASSIFIED SECTION

• Lubricant

• Relieves Dry Eyes

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

Eye04Eye04

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73921-004-152023-02-08C16284748780-1f386c649-bfa4-0266-e053-dadaa90a7c1ai-Drops ARTIFICIAL TEARS
73921-004-152023-01-30C16284748780-1f386c649-bfa4-0266-e053-dadaa90a7c1ai-Drops ARTIFICIAL TEARS

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73921-00473921-004-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
f42b51b2-318e-eb6f-e053-2995a90a56d64a721be0-6123-4879-b428-be0a5319e68e2023-02-08WarningsExact identifier
spl set id: 4a721be0-6123-4879-b428-be0a5319e68e

Reported adverse events (FAERS/openFDA)#

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