Label: MEDI-FIRST FIRST AID EYE WASH- purified water solution

  • NDC Code(s): 47682-197-11, 47682-197-26, 47682-198-08, 47682-198-11, view more
    47682-198-18, 47682-198-26, 47682-198-28
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated January 16, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Purified water 98.3%

  • Purpose

    Eyewash

  • Use

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

  • Warnings

    For external use only

    Do not use

    • if you experience any open wounds in or near the eyes and obtain immediare 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 experience

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

    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 20º to 25º C [68º to 77º 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 800-634-7680

  • Medi-First Eye Wash Label

    Medi-First®

    Purified Water, 98.3%

    Ophthalmic Solution

    Eyewash

    NDC 47682-197-11

    Single Use

    Manufactured for

    Medique Products

    17080 Alico Commerce Ct.

    Fort Myers, FL 33967

    Made in Canada

    Reorder #21511

    Sterile Solution

    16 fl oz [473 mL]

    MF Eyewash 16 oz

  • Medi-First Eyewash Label

    NDC 47682-198-28

    Medi-First®

    Eyewash

    Sterile Solution

    1 fl oz bottle (1)

    (98.3% Purified water, use to cleanse eyes)

    Reorder #1981B

    MF Eyewash 1 oz box

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST FIRST AID EYE WASH 
    purified water solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-198
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER983 mg  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:47682-198-18118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/02/2011
    2NDC:47682-198-08236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/02/2011
    3NDC:47682-198-11473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/02/201109/30/2015
    4NDC:47682-198-26946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/02/201112/31/2015
    5NDC:47682-198-2830 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/02/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02230512/02/2011
    MEDI-FIRST FIRST AID EYE WASH 
    purified water solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-197
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER983 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    BORIC ACID (UNII: R57ZHV85D4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-197-11473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product10/01/2015
    2NDC:47682-197-26946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02230510/01/2015
    Labeler - Unifirst First Aid Corporation (832947092)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!