Label: EQUATE SUPPORT ADVANCED LUBRICANT DROPS MULTIDOSE- polyethylene glycol 400, propylene glycol solution/ drops

  • 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 April 18, 2018

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  • SPL UNCLASSIFIED SECTION

    Walmart

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    Lubricant Gel Drops Multi-Dose

    Preservative Free 7.5mL

    NDC 49035-878-52

    Drug Facts

  • Active ingredients

    Polyethylene Glycol 400 0.4%

    Propylene Glycol 0.3%

  • Purpose

    Lubricant

    Lubricant

  • Uses

    • Relieves dryness of the eye.
    • For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to the wind and sun
    • May be used as a protectant against further irritation.
  • Warnings

    • For use in the eyes only.  Retain outer carton for full product drug facts.

    Do not use

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

    When using this product

    • do not touch tip of container to any surface avoid contamination.
    • remove contact lenses
    • replace cap after each use.
    • do not deliver more than 6 consecutive drops.

    Stop use and ask a doctor if  

    • you feel eye pain.
    • changes in vision occur.
    • redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours.

    Keep this and all drugs out of the 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.

    1. Twist Open 2. Squeeze

  • Other information

    • Store at room temperature 15°-30°C (59°-86°F).
  • Inactive ingredients

    Aminomethylpropanol, boric acid, gellan gum, magnesium chloride hexahydrate, potassium chloride, purified water, sodium chloride, sorbitol. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

  • Questions and comments?

    • 1 (888) 287-1915
  • PRINCIPAL DISPLAY PANEL

    NDC 49035-878-52
    equate
    Support Advanced
    Lubricant
    Gel Drops
    Multi-Dose
    Preservative Free
    Sterile
    0.25 FL OZ (7.5mL)

    PRINCIPAL DISPLAY PANEL
NDC 49035-878-52
equate
Support Advanced
Lubricant 
Gel Drops 
Multi-Dose 
Preservative Free
Sterile
0.25 FL OZ (7.5mL)

  • INGREDIENTS AND APPEARANCE
    EQUATE SUPPORT ADVANCED LUBRICANT DROPS MULTIDOSE 
    polyethylene glycol 400, propylene glycol solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-878
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4004.0 mg  in 1 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL3.0 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    BORIC ACID (UNII: R57ZHV85D4)  
    GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SORBITOL (UNII: 506T60A25R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-878-527.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart34906/01/2018
    Labeler - Wal-Mart Stores, Inc. (051957769)
    Registrant - Altaire Pharmaceuticals, Inc. (786790378)