Label: LIPOSOMAL HEMORRHOID MASTER- lidocaine hcl 4%, phenylephrine hcl 0.25% ointment

  • NDC Code(s): 84735-008-01
  • Packager: Hengyang Chuangjiujia Trading Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated May 12, 2025

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Lidocaine HCl 4%

    Phenylephrine HCl 0.25%

  • PURPOSE


    Loca Anesthetic
    Vasoconstrictor

  • INDICATIONS & USAGE


    Uses. Forthe temporany relief of local and anorectal iching and discomfot asociated with anoreclal isorders and anorectalimammation.
    Forthe temporany reief of pain,buring and sorenes.
    Temporarily shrinks hemorthoidal tisue, Temporarily reduces the sweling associated with iritation in hemorthoids and other anorectal disorders.

  • WARNINGS

    For external and /or intrarectal use only.

  • DO NOT USE


    Do not use this product if you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.
    Ask a doctor or pharmacist before use if you are presently taking a prescription drug for high blood pressure or depression.
    Do not use this product with an applicator if the introduction of the applicator into the rectum causes additional pain. Consult a doctor promptly.

  • WHEN USING


    If condition worsens or does not improve within 7 days, consult a doctor.
    Do not exceed the recommended daily dosage unless directed by a doctor.
    In case of bleeding, consult a doctor promptly.

  • STOP USE

    Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep away from direct sunlight or heat.

  • DOSAGE & ADMINISTRATION

    Directions: Adults: 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. Children under 12 years of age: consult a doctor.

  • INACTIVE INGREDIENT

    Petrolatum
    Aloe Barbadensis Leaf Extract
    Glycerin
    Mineral Oil
    Chamomilla Recutita (Matricaria) Flower Extract
    Tocopherol
    Ascorbic Acid
    Pyridoxine HCl
    Ginseng Extract
    Propylene Glycol
    Sodium Hyaluronate
    Polysorbate 80
    Panthenol
    Allantoin
    Phenoxyethanol
    Ethylhexylglycerin
    Carbomer
    Triethanolamine
    Water

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    LIPOSOMAL HEMORRHOID MASTER 
    lidocaine hcl 4%, phenylephrine hcl 0.25% ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84735-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    PHENYLEPHRINE (UNII: 1WS297W6MV) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE0.25 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    PYRIDOXINE HCL (UNII: 68Y4CF58BV)  
    CHAMOMILE (UNII: FGL3685T2X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    TRIETHANOLAMINE (UNII: 9O3K93S3TK)  
    ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CARBOMER (UNII: 0A5MM307FC)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84735-008-0150 g in 1 TUBE; Type 0: Not a Combination Product05/12/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/12/2025
    Labeler - Hengyang Chuangjiujia Trading Co., Ltd. (977292157)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hengyang Chuangjiujia Trading Co., Ltd.977292157manufacture(84735-008)