OASIS TEARS  LUBRICANT EYE- glycerin solution/ drops 
OASIS Medical, 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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OASIS Tears®
Lubricant Eye Drops

Drug Facts

Active Ingredients

Glycerin (0.22%)

Purpose

lubricant Eye Drops

Uses

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

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

Directions

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

Questions, or to report an adverse event call:

(800) 631-7180 or (909) 305-5400 or log onto www.oasistears.com

Other information

Inactive Ingredients

EDTA, potassium sorbate, sodium chloride, sodium hyaluronate, sodium hydroxide, sodium phosphate dibasic, sodium phosphate monobasic, water

PRINCIPAL DISPLAY PANEL - 10mL Bottle Carton

Oasis

TEARS
®



LUBRICANT EYE DROPS

VISCOADAPTIVE...RELIEF

FOR DRY EYES

10mL/0.3 fl. oz.

OASIS TEARS

OASIS TEARS   LUBRICANT EYE
glycerin solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42126-6310
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)  
SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:42126-6310-11 in 1 CARTON01/09/2010
110 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/09/2010
Labeler - OASIS Medical, Inc. (194121018)
Establishment
NameAddressID/FEIBusiness Operations
Excelvision274234566pack(42126-6310) , manufacture(42126-6310)

Revised: 2/2018
Document Id: fdbf7d44-f8a3-4109-a9b2-3ee48b78b9df
Set id: 00071697-4ac6-4962-8eee-388b8b52bd40
Version: 4
Effective Time: 20180202
 
OASIS Medical, Inc.