OCUSAN DRY EYES- polyethylene glycol 400, propylene glycol liquid 
DLC Laboratories, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Ocusan ® Dry Eyes

Drug Facts

Active ingredientsPurposes
Polyethylene Glycol 400 0.4%Lubricant
Proplyene Glycol 0.3%Lubricant

Use

Warnings

For external use only

Do Not Use

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

When using this product

  • 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 experience any of the following:

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye
  • condition worsens 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

Other information

Inactive ingredients

benzalkonium chloride, boric acid, hydrochloric acid, hypromellose, potassium chloride, sodium chloride, sodium hydroxide, water for injection

Questions

1-800-858-3889

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

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Box

Advanced Formula!

Fase Acting


Ocusan ®

Dry Eyes

Moisturizes & Soothes Dry Eyes



Lubricant Eye Drops / Relieves Buring and Irritation

STERILE

1/2 FL OZ (15 mL)

carton

OCUSAN DRY EYES 
polyethylene glycol 400, propylene glycol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1292
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL3 mg  in 1 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ, POLYETHYLENE GLYCOL, UNSPECIFIED - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 4004 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
BORIC ACID (UNII: R57ZHV85D4)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1292-51 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 finalpart34912/16/2019
Labeler - DLC Laboratories, Inc. (093351930)

Revised: 1/2023
Document Id: f22dd8e5-05b8-61b2-e053-2995a90a457b
Set id: a5b9209c-0187-9d5e-e053-2a95a90a20a6
Version: 2
Effective Time: 20230113
 
DLC Laboratories, Inc.