Label: EQUATE NIGHTTIME RELIEF LUBRICANT- light mineral oil, white petrolatum ointment

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 1, 2024

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  • Active ingredients

    Light Mineral Oil 42.5%

    White Petrolatum 57.3%

  • Purposes

    Eye Lubricant

    Eye Lubricant

  • Uses

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

    For external use only

    Do not use

    • except under the advice and supervision of a doctor

    When using this product

    • replace cap after use
    • to avoid contamination do not touch tip of container to any surface
    • remove contact lenses before using

    Stop use and ask a doctor if

    • you experience eye pain, changes in vision, continued redness or irritation of the eye
    • 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 (1-800-222-1222) right away.

  • Directions

    • pull down the lower lid of the affected eye
    • apply a small amount (1/4 inch) of ointment to the inside of eyelid
  • Other information

  • Inactive ingredient

    lanolin alcohols

  • Questions or comments?

    Call 1-888-287-1915

  • Equate Eye Ointment Nighttime Relief Lubricant 3.5g

    Equate Eye Ointment Nighttime Relief Lubricant 3.5g

  • INGREDIENTS AND APPEARANCE
    EQUATE NIGHTTIME RELIEF LUBRICANT 
    light mineral oil, white petrolatum ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-260
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIGHT MINERAL OIL (UNII: N6K5787QVP) (LIGHT MINERAL OIL - UNII:N6K5787QVP) LIGHT MINERAL OIL425 mg  in 1 g
    WHITE PETROLATUM (UNII: B6E5W8RQJ4) (WHITE PETROLATUM - UNII:B6E5W8RQJ4) WHITE PETROLATUM573 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-260-351 in 1 BOX04/01/2024
    13.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01804/01/2024
    Labeler - Walmart Inc. (051957769)
    Registrant - KC Pharmaceuticals, Inc. (174450460)
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