Label: MAYINGLONG HEMORRHOIDAL- petrolatum, zinc oxide ointment

  • NDC Code(s): 68511-998-01, 68511-998-02
  • Packager: Mayinglong Pharmaceutical Group Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 8, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredients

    Petrolatum 77.99%

    Calamine 7.6%

    Purpose

    Protectant

    Astringent

  • Uses

    • For the temporary relieve of local itching and discomfort associated with hemorrhoids.
    • Temporarily forms a protective coating over inflamed tissues to help prevent drying of tissues.
    • Temporarily protects irritated areas.
    • Temporarily relieves burning.
    • Provides temporary relief from skin irritations.
    • Temporarily provides a coating for relief of anorectal discomforts.
    • Temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful.
    • Temporarily protects inflamed perianal skin.
    • Temporarily relieves the symptoms of perianal skin irritation.
  • Warnings

    For external use and/or intrarectal use only

    Do not use

    • If allergic to any of the ingredients

    When using this product

    • Do not exceed the recommended daily dosage unless as directed by a doctor.
    • Do not use the product with an applicator if the introduction of the applicator into the rectum causes additional pain. Consult a doctor promptly.

    Stop use and ask a doctor if

    • Bleeding occurs 
    • Condition worsens or does not improve within 7 days

    Do not use during pregnancy or when breast feeding.

    Consult a health professional before use.

    Keep out of reach of children

    to avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away Do not use otherwise than as directed.

  • Directions

    • Adults: When practical, cleanse the affected area with mild soap and warm water, rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of the ointment.
    • Apply to the affected area up to 2 times daily or after each bowel movement.
    • Apply liberally to the affected area.
    • Attach applicator to tube. Lubricate applicator well with ointment, then gently insert applicator into the rectum. FOR INTRARECTAL USE:
    • Children under 12 years of age: consult a doctor.
  • Other information

    • Store at room temperature, 10 ℃ to 30℃ (50℉ to 86℉)
    • Keep the container closed tightly
  • Inactive ingredients

    Amber, Artificial bezoar (Bos Taurus Bile, Cholic Acid,D eoxycholic Acid, Taurine, Bilirubin, Cholesterol), Artificial musk (Muscone), Borax, Borneol, Dimethyl sulfoxide, Lanolin, Pear

  • Questions?

    +1-888-915-6789 M-F 9am to 5pm Pacific Time You may report serious side effects to this phone number.

  • Package Labeling:

    Label

  • Package Labeling:

    BottleBottle2

  • INGREDIENTS AND APPEARANCE
    MAYINGLONG HEMORRHOIDAL 
    petrolatum, zinc oxide ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68511-998
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM779.9 mg  in 1 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION76 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    AMBER (UNII: 70J9Z0J26P)  
    BOS TAURUS BILE (UNII: ET3651ZLOU)  
    CHOLIC ACID (UNII: G1JO7801AE)  
    DEOXYCHOLIC ACID (UNII: 005990WHZZ)  
    TAURINE (UNII: 1EQV5MLY3D)  
    BILIRUBIN (UNII: RFM9X3LJ49)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    MUSCONE (UNII: UPS3C6CV36)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    BORNEOL (UNII: M89NIB437X)  
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
    LANOLIN (UNII: 7EV65EAW6H)  
    PEARL (HYRIOPSIS CUMINGII) (UNII: A75L5FZ40U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68511-998-011 in 1 BOX08/01/2018
    110 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:68511-998-021 in 1 BOX08/01/2018
    210 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01508/01/2018
    Labeler - Mayinglong Pharmaceutical Group Co., Ltd. (526823828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mayinglong Pharmaceutical Group Co., Ltd.526823828manufacture(68511-998)