REAL EYEWASH- eyewash solution 
Oliver Landon Intl Inc.

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Real Eyewash
Drug Facts

Active ingredient

Purified water 98.3%

Purpose

Eyewash

Warnings

For external use only

Do not use

if you experience any open wounds in or near the eyes and obtain immediate medical treatment
if solution changes color or becomes cloudy

When using this product

to avoid contamination, do not touch tip of container to any surface
do not reuse
once opened, discard

Stop use and ask a doctor if you have any of the following

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

Use

For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Keep out of reach of children

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

Directions

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

Other information

lot number is printed on the bottle
store at 20° to 25° C [68° to 77° F)
for your protection, this bottle has an imprinted white seal with black printing “TAMPER EVIDENT SEAL”
do not use if this seal is missing or broken
use before expiration date marked on bottle

Inactive ingredients

boric acid, sodium borate, sodium chloride

Questions?

Call (800) 839-5929   9 a.m. to 5 p.m. EST Mon-Fri

Package/Label Principal Display Panel – 1 FL OZ (30 mL) label

Real Eyewash 1 FL OZ (30 mL) front label
Real Eyewash 1 FL OZ (30 mL) back label

Package/Label Principal Display Panel – 4 FL OZ (118 mL)

Real Eyewash 4 FL OZ (118 mL) label

Package/Label Principal Display Panel – 8 FL OZ (236 mL)

Real Eyewash 8 FL OZ (236 mL) label

Package/Label Principal Display Panel – 16 FL OZ (473 mL)

Real Eyewash 16 FL OZ (473 mL) label

Package/Label Principal Display Panel – 32 FL OZ (946 mL)

Real Eyewash 32 FL OZ (946 mL) label
REAL EYEWASH 
eyewash solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59276-416
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER0.983 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59276-416-0130 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product09/01/2015
2NDC:59276-416-04118 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product09/01/2015
3NDC:59276-416-08236 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product09/01/2015
4NDC:59276-416-16473 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product09/01/2015
5NDC:59276-416-32946 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product09/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02230501/30/2015
Labeler - Oliver Landon Intl Inc. (815240195)
Registrant - Oliver Landon Intl Inc. (815240195)
Establishment
NameAddressID/FEIBusiness Operations
Niagara Pharmaceuticals, Inc.205477792MANUFACTURE(59276-416)

Revised: 10/2019
Document Id: 713cf5aa-b2f4-442a-abdb-47f107c5faa3
Set id: 713cf5aa-b2f4-442a-abdb-47f107c5faa3
Version: 1
Effective Time: 20191022
 
Oliver Landon Intl Inc.