Health Mart Dry Eye Relief Lubricant Eye Drops

Manufacturer: Strategic Sourcing Services LLC | KC Pharmaceuticals, Inc.
Effective date: 2024-07-14
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 20:59:07

Label at a glance#

ProductHealth Mart Dry Eye Relief Lubricant Eye Drops

Active ingredientHYPROMELLOSES, GLYCERIN, POLYETHYLENE GLYCOL 400

Label structure8 sections

Indications and uses

for the temporary relief of burning and irritation due to dryness of the eye for protection against further irritation

Dosage and administration

Instill 1 or 2 drops in the affected eye(s) as needed Children under 6 years of age, ask doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Glycerin 0.2%

Hypromellose 0.2%

Polyethylene glycol 1%

Purpose

OTC - PURPOSE SECTION

Glycerin.....Lubricant

Hypromellose.....Lubricant

Polyethylene glycol 400.....Lubricant

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of burning and irritation due to dryness of the eye
for protection against further irritation

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

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 worsen or persists for more than 72 hours

OTC - WHEN USING SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant and breast-feeding, ask a health professional before use

Directions

DOSAGE & ADMINISTRATION SECTION

Instill 1 or 2 drops in the affected eye(s) as needed
Children under 6 years of age, ask doctor

Other information

OTHER SAFETY INFORMATION

RETAIN THIS CARTON FOR FUTURE REFERENCE

Store at 15 ^oC-30 ^oC (59 ^o-88 ^oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

dextrose, sodium chloride, potassium chloride, sodium phosphate monobasic, sodium phosphate dibasic, sodium bicarbonate, sodium citrate, edetate disodium, benzalkonium chloride, purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62011-0196-1	ML - Milliliter	62011-0196	2936effc-479f-4972-82bd-fa2cd4267495	1	2014-10-03

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

Health Mart Dry Eye Relief Lubricant Eye Drops
Glycerin, Hypromellose, Polyethylene glycol 400
SODIUM CHLORIDE
SODIUM PHOSPHATE, MONOBASIC
POTASSIUM CHLORIDE
SODIUM PHOSPHATE, DIBASIC
SODIUM BICARBONATE
SODIUM CITRATE
EDETATE DISODIUM
BENZALKONIUM CHLORIDE
WATER
HYPROMELLOSES
HYPROMELLOSE, UNSPECIFIED
GLYCERIN
POLYETHYLENE GLYCOL 400
DEXTROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62011-0196	62011-0196-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM PHOSPHATE, MONOBASIC	3980JIH2SW	IACT
POTASSIUM CHLORIDE	660YQ98I10	IACT
SODIUM PHOSPHATE, DIBASIC	GR686LBA74	IACT
SODIUM BICARBONATE	8MDF5V39QO	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
WATER	059QF0KO0R	IACT
HYPROMELLOSES	3NXW29V3WO	ACTIB
GLYCERIN	PDC6A3C0OX	ACTIB
POLYETHYLENE GLYCOL 400	B697894SGQ	ACTIB
DEXTROSE	IY9XDZ35W2	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1d34f2c2-4e37-0246-e063-6294a90a287b			5ba9c3e3-e5b9-4bdd-ba08-d1fa3e65c089	2024-07-14	Warnings	Exact identifier spl id: 1d34f2c2-4e37-0246-e063-6294a90a287b spl set id: 5ba9c3e3-e5b9-4bdd-ba08-d1fa3e65c089

Reported adverse events (FAERS/openFDA)#

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