Label: HEMORRHOID RELIEF CREAM- lidocaine cream

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

Drug Label Information

Updated April 20, 2024

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  • Active ingredient

    Lidocaine 5% w/w

  • Purpose

    Local anesthetic

  • Uses

    helps relieve the pain, itching, and burning associated with hemorrhoids and other anorectal disorders

  • Warnings

    For external use only

    When using this product

    • avoid contact with eyes
    • do not put this product into the rectum by using fingers or any mechanical device or applicator
    • do not exceed the recommended daily dosage unless directed by a doctor

    Stop use and ask a doctor if

    • rectal bleeding occurs
    • an allergic reaction develops to ingredients in this product
    • condition worsens or does not improve within 7 days
    • symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.
    • adults and children 12 years and over: apply externally to the affected area up to 6 times daily
    • children under 12 years: consult a doctor
  • Other information

    • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
    • see end flap for expiration date and lot number
  • Inactive ingredients

    aloe barbadensis leaf juice, benzyl alcohol, carbomer, cholesterol, hydrogenated lecithin, isopropyl myristate, polysorbate 80, propylene glycol, purified water, triethanolamine, vitamin E acetate, vitis vinifera (grape) skin extract

  • Questions or comments?

    1-888-287-1915

  • Principal display panel

    NDC 49035-717-43

    equate™

    Compare to
    RectiCare®
    Active
    Ingredient*

    Hemorrhoid
    Relief Cream

    Lidocaine 5%
    Anorectal Cream

    • Helps relieve pain and burning

    • For the temporary relief of itching and
    discomfort associated with hemorrhoids
    and other anorectal disorders

    • Highest lidocaine strength
    available over-the-counter

    NET WT 1 OZ (30 g)

    TAMPER EVIDENT: DO NOT
    USE IF FOIL SEAL UNDER
    CAP IS BROKEN OR
    MISSING OR TUBE IS
    DAMAGED

    Satisfaction guaranteed
    – Or we’ll replace it or
    give you your money
    back. For questions or
    comments or to report
    an undesired reaction
    or side effect, please
    call 1-888-287-1915.

    DISTRIBUTED BY:
    Walmart Inc.,
    Bentonville, AR 72716

    *This product is not
    manufactured or distributed
    by Ferndale IP, Inc., owner of
    the registered trademark
    RectiCare®.

    50844 ORG121871743

    Equate 44-717

    Equate 44-717

  • INGREDIENTS AND APPEARANCE
    HEMORRHOID RELIEF CREAM 
    lidocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-717
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VITIS VINIFERA ANTHOCYANINS (UNII: F02KPB2508)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-717-431 in 1 CARTON04/30/2019
    130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01504/30/2019
    Labeler - Wal-Mart Stores Inc (051957769)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.038154464pack(49035-717)
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