OCTIQ LUBRICANT EYE DROPS- dextran 70 hypromellose solution/ drops

Octiq Lubricant Eye Drops by

Drug Labeling and Warnings

Octiq Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Innovus Pharmaceuticals, Inc., AMMAN PHARMACEUTICAL INDUSTRIES. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Dextran 70 0.1%

Hypromellose 2910 0.3%

Purpose

Lubricant

Lubricant

Uses

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

Warnings

For external use only

Do not use

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

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 feel eye pain
• changes in vision occur redness or irritation of the eye gets worse or lasts more than 72 hours

Keep out of reach of children 

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

Directions

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

Other Information 

• Store at room temperature

Inactive ingredients

Boric acid, disodium edetate, potassium chloride, povidone, purified water, sodium borate, sodium chloride
Preservative added: benzalkonium choride

Questions?

Call 1.800.996.5122

(Mon-Fri 9AM-5PM EST)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

OCTIQ LUBRICANT EYE DROPS 
dextran 70 hypromellose solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57483-610
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68)	DEXTRAN 70	1 mg  in 1 mL
HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (HYPROMELLOSE 2910 (4000 MPA.S) - UNII:RN3152OP35)	HYPROMELLOSE 2910 (4000 MPA.S)	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
POVIDONE (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57483-610-15	2 in 1 CARTON	11/14/2021
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M	11/14/2021

Labeler - Innovus Pharmaceuticals, Inc. (962507187)

Establishment
Name	Address	ID/FEI	Business Operations
AMMAN PHARMACEUTICAL INDUSTRIES		534677849	manufacture(57483-610)