Label: MEIJER LUBRICANT SINGLE VIAL- carboxymethylcellulose sodium solution/ drops

  • NDC Code(s): 41250-582-30, 41250-582-70
  • Packager: Meijer, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated June 25, 2019

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

  • ACTIVE INGREDIENT

    Active ingredients                                                                 Purpose

    Carboxymethylcellulose Sodium 0.5%.................................. Eye Lubricant

  • PURPOSE

    Uses

    • for the temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun
    • may be used as protectant against further irritation
  • WARNINGS

    Warnings

    For external use only.

    • do not touch tip of container to any surface to avoid contamination
    • do not reuse
    • once opened, discard
    • do not use if solution changes color or becomes cloudy
    • remove contact lenses before using
  • STOP USE

    Stop use and ask a doctor if you experience eye pain, changes in visiion, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • INDICATIONS & USAGE

    Directions

    • to open, twist and pull tab to remove
    • instill 1 or 2 drops in the affected eye(s) as needed
    • children under 6 years of age: ask a doctor
  • CALIBRATION INSTRUCTIONS

    Other information

    • store between 15-30°C (59-86°F)
    • protect from light
  • INACTIVE INGREDIENT

    Inactive ingredients calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide, sodium lactate.

  • DOSAGE & ADMINISTRATION

    DISTRIBUTED BY:

    MEIJER DISTRIBUTION, INC.

    GRAND RAPIDS, MI 49544

    Made in Korea

  • PRINCIPAL DISPLAY PANEL

    94358

  • PRINCIPAL DISPLAY PANEL

    94359

  • INGREDIENTS AND APPEARANCE
    MEIJER LUBRICANT SINGLE VIAL 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-582
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-582-3030 in 1 CARTON02/03/2015
    10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    2NDC:41250-582-7070 in 1 CARTON02/03/2015
    20.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34902/03/2015
    Labeler - Meijer, Inc. (006959555)