Lubricating Eye Drops

Manufacturer: Rugby Laboratories | Velocity Pharma LLC
Effective date: 2022-11-20
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 21:47:27

Label at a glance#

ProductLubricating Eye Drops

Active ingredientDEXTRAN 70, HYPROMELLOSE 2910 (4000 MPA.S)

Label structure12 sections

Indications and uses

temporary relief of burning and irritation due to dryness of the eye temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun as a protectant against further irritation

Dosage and administration

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

Storage and handling

store at room temperature

Contacts and useful links#

PhoneLabel contact1-800-645-2158

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

*Active Ingredients*	*Purpose*
Dextran 70 0.1%	Lubricant
Hypromellose 2910 0.3%	Lubricant

Uses

INDICATIONS & USAGE SECTION

temporary relief of burning and irritation due to dryness of the eye
temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
as a protectant against further irritation

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if solution changes color or becomes cloudy
if you are sensitive to any ingredient in this product

When using this product

OTC - WHEN USING SECTION

to avoid contamination, do not touch tip of container to any surface
replace cap after using

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience any of the following:

eye pain
changes in vision
continued redness or irritation of the eye
condition worsens or persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive ingredients:

INACTIVE INGREDIENT SECTION

boric acid, calcium chloride, glycerin, glycine, magnesium chloride, polysorbate 80, potassium chloride, purified water, sodium borate, sodium chloride, stabilized oxychoro complex, zinc chloride. May contain hydrocholric acid and/or sodium hydroxide to adjust pH.

Questions?

OTC - QUESTIONS SECTION

Call 1-800-645-2158

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0536-1282-94	ML - Milliliter	0536-1282	cf8f6c43-9026-47bd-af4c-f58c875724b2	1	2021-06-02

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

Lubricating Eye Drops
dextran 70 and hypromellose 2910
BORIC ACID
CALCIUM CHLORIDE
GLYCERIN
GLYCINE
MAGNESIUM CHLORIDE
POLYSORBATE 80
POTASSIUM CHLORIDE
WATER
SODIUM BORATE
SODIUM CHLORIDE
SODIUM CHLORITE
ZINC CHLORIDE
HYDROCHLORIC ACID
SODIUM HYDROXIDE
DEXTRAN 70
HYPROMELLOSE 2910 (4000 MPA.S)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0536-1282	0536-1282-94

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BORIC ACID	R57ZHV85D4	IACT
CALCIUM CHLORIDE	M4I0D6VV5M	IACT
GLYCERIN	PDC6A3C0OX	IACT
GLYCINE	TE7660XO1C	IACT
MAGNESIUM CHLORIDE	02F3473H9O	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
POTASSIUM CHLORIDE	660YQ98I10	IACT
WATER	059QF0KO0R	IACT
SODIUM BORATE	91MBZ8H3QO	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM CHLORITE	G538EBV4VF	IACT
ZINC CHLORIDE	86Q357L16B	IACT
HYDROCHLORIC ACID	QTT17582CB	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
DEXTRAN 70	7SA290YK68	ACTIB
HYPROMELLOSE 2910 (4000 MPA.S)	RN3152OP35	ACTIB

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
0fa853a8-61aa-5e6d-e063-6294a90a38ee			f5712fe5-fb2b-4c7d-865e-d3984bb5c4e4	2024-01-23	Warnings	Exact identifier spl set id: f5712fe5-fb2b-4c7d-865e-d3984bb5c4e4

Reported adverse events (FAERS/openFDA)#

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