Octiq Lubricant Eye  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]

OCTIQ LUBRICANT EYE DROPS- dextran 70 hypromellose solution/ drops 
Innovus Pharmaceuticals, Inc.

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Octiq Lubricant Eye  Drops

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)

image description

OCTIQ LUBRICANT EYE DROPS 
dextran 70 hypromellose solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 57483-610
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 701 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 NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 57483-610-152 in 1 CARTON11/14/202110/31/2024
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM11/14/202110/31/2024
Labeler - Innovus Pharmaceuticals, Inc. (962507187)
Establishment
NameAddressID/FEIBusiness Operations
AMMAN PHARMACEUTICAL INDUSTRIES534677849manufacture(57483-610)

Revised: 7/2024