i-Drops LUBRICANT EYE DROPS

Manufacturer
GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Effective date
2021-03-26
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 LUBRICANT EYE DROPS
Active ingredientGLYCERIN
Label structure10 sections

Indications and uses

• For use as a lubricant to prevent 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 in the refrigerator  do not freeze store in dark, cool place away from sunlight once open, discard container and any content after 30 days use before expiration date marked on container prior to drop instillation, contact lenses should be removed and reinserted after 10 minutes

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Glycerin 1.0%

PURPOSE

OTC - PURPOSE SECTION

lubricant

Uses

INDICATIONS & USAGE SECTION

• For use as a lubricant to prevent 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 if solution changes color or becomes cloudy

When using this product
• To avoid contamination, do not touch tip of container to any surface
• replace cap after using

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 or persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If product is 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 in the refrigerator 

do not freeze

store in dark, cool place away from sunlight

once open, discard container and any content after 30 days

use before expiration date marked on container

prior to drop instillation, contact lenses should be removed and reinserted after 10 minutes

Inactive ingredients

INACTIVE INGREDIENT SECTION

Boric acid, Citric acid, Hypromellose, Potassium bicarbonate, Purified benzyl alcohol, Sterile water

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

i-Drops06i-Drops06

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73921-006-152023-02-08C16284748780-1f386c64a-19a9-0266-e053-dadaa90a7c1ai-Drops LUBRICANT EYE DROPS
73921-006-152023-01-30C16284748780-1f386c64a-19a9-0266-e053-dadaa90a7c1ai-Drops LUBRICANT EYE DROPS

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73921-00673921-006-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
f42b6382-057f-0e63-e053-2a95a90a211c22e8e404-7ecb-4f2d-bfc7-6ce8d4a333e72023-02-08WarningsExact identifier
spl set id: 22e8e404-7ecb-4f2d-bfc7-6ce8d4a333e7

Reported adverse events (FAERS/openFDA)#

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