Label: EQUATE HEMORRHOID RELIEF- lidocain 5% cream

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

Drug Label Information

Updated March 11, 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 anorectal disorders.

  • WARNINGS

    For external use only

    When using this product

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

    Stop use and ask a doctor if

    • rectal bleeding occurs
    • condition worsens or does not improve within 7 days
    • symptoms clear up and occur again within a few days
    • an allergic reaction develops to ingredients in this product
    • 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 and pets.

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

  • DIRECTIONS

    Adult and children 12 years and over:

    • 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.
    • apply externally to the affected area up to 6 times a day

    children under 12 years of age: consult a doctor.

  • OTHER INFORMATION

    Store between 15°-30° C (59°-30° F)

  • INACTIVE INGREDIENTS

    Benzyl Alcohol, Carbomer 940, Cholesterol, Isopropyl Myristate, Lecithin (Soya), Polysorbate 80, Propylene Glycol, Purified Water, Triethanolamine, Vitamin-E Acetate

  • QUESTIONS

    1-888-287-1915

  • PRINCIPAL DISPLAY PANEL

    PRINCIPAL DISPLAY PANEL

  • INGREDIENTS AND APPEARANCE
    EQUATE HEMORRHOID RELIEF 
    lidocain 5% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-109
    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
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-109-301 in 1 CARTON04/01/2022
    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 DrugM01504/01/2022
    Labeler - WALMART, INC (051957769)
    Registrant - GURUNANDA, LLC (079671169)
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