FDA.reportPublic FDA data

i-Drops LUBRICANT EYE DROPS

Manufacturer
GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Effective date
2021-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:48:13

Label at a glance#

Producti-Drops LUBRICANT EYE DROPS
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Label structure10 sections

Indications and uses

For use as a protectant against further irritation or to relieve dryness of the eye. For the relief of discomfort due to minor irritations of the eye or to exposure to wind, sun or screen time.

Dosage and administration

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

Storage and handling

Tamper Evident. Do not use this product if neckband is missing or broken. RETAIN THIS CARTON FOR FUTURE REFERENCE. Store at 15°-30°C (59° to 86°F).

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose Sodium 10mg in 1 ml.

PURPOSE

OTC - PURPOSE SECTION

Eye lubricant

Uses

INDICATIONS & USAGE SECTION

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

For the relief of discomfort due to minor irritations of the eye or to exposure to wind, sun or screen time.

Warnings

WARNINGS SECTION

For external use only.

Do not use product if solution changes color or becomes cloudy.

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.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

Tamper Evident. Do not use this product if neckband is missing or broken.

RETAIN THIS CARTON FOR FUTURE REFERENCE.

Store at 15°-30°C (59° to 86°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Boric Acid, Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Magnesium Chloride, Sodium Hydroxide and Water for Injection.

Questions?

OTC - QUESTIONS SECTION

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

SPL UNCLASSIFIED SECTION

Immediate relief for dry eyes

Long lasting moisture rich formula

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

idrops02-1idrops02-1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73921-002-152023-02-08C16284748780-1f386c64a-1e0d-0266-e053-dadaa90a7c1ai-Drops LUBRICANT EYE DROPS
73921-002-152023-01-30C16284748780-1f386c64a-1e0d-0266-e053-dadaa90a7c1ai-Drops LUBRICANT EYE DROPS

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73921-00273921-002-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311ACTIB
BORIC ACIDR57ZHV85D4IACT
POTASSIUM CHLORIDE660YQ98I10IACT
SODIUM CHLORIDE451W47IQ8XIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT

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-6d82-2a78-e053-2a95a90a342acad56a48-05fe-449a-af63-519f073a15332023-02-08WarningsExact identifier
spl set id: cad56a48-05fe-449a-af63-519f073a1533

Reported adverse events (FAERS/openFDA)#

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