COLIRIO OCUSAN- tetrahydrozoline hydrochloride, polyethylene glycol 400, povidone, unspecified, and dextran 70 liquid 
DLC Laboratories, Inc.

----------

Colirio Ocusan ®

Drug Facts

Active ingredientsPurposes
Dextran 70 0.1%Lubricant
Polyethylene Glycol 400 1%Lubricant
Povidone 1%Lubricant
Tetrahydrozoline HCl 0.05%Redness reliever

Use

Warnings

For external use only

Ask a doctor before use if you havenarrow angle glaucoma.

When using this product

  • pupils may become enlarged temporarily
  • overuse may cause more eye redness
  • remove contact lenses before using
  • do not use if this solution changes color or becomes cloudy
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts
  • condition worsens or lasts more than 72 hours

If pregnant or breastfeeding,ask a health professional before use.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

benzalkonium chloride, boric acid, disodium edetate hydrate, sodium borate, sodium chloride, water for injection

Questions

1-800-858-3889

Distributed by:
DLC LABORATORIES, INC.
PARAMOUNT, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Box

Improved Formula!

Now
with
3
Moisturizers

Maximum
Strength

Colirio
Ocusan ®

Fast Redness Relief
Soothes & Lubricates

Redness Reliever /
Lubricant Eye Drops

STERILE

1/2 FL OZ (15 mL)

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Box
COLIRIO OCUSAN 
tetrahydrozoline hydrochloride, polyethylene glycol 400, povidone, unspecified, and dextran 70 liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1575
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ, POLYETHYLENE GLYCOL, UNSPECIFIED - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 40010 mg  in 1 mL
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E) POVIDONE, UNSPECIFIED10 mg  in 1 mL
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 701 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1575-11 in 1 BOX12/16/2019
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01812/16/2019
Labeler - DLC Laboratories, Inc. (093351930)
Registrant - DLC Laboratories, Inc. (093351930)

Revised: 4/2025
Document Id: 2f3841d0-c77b-aa79-e063-6294a90a53c1
Set id: 0f0dd0bd-9a35-4671-933a-f3f8e834ae65
Version: 5
Effective Time: 20250418
 
DLC Laboratories, Inc.