Label: MAYINGLONG HEMORRHOIDS- zinc oxide, petrolatum, lanolin ointment

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated March 20, 2018

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  • Active Ingredients

    Zinc Oxide 0.8g Astrigent

    Petrolatum 7.85g Protectant

  • Purpose

    Astrigent

    Protectant

    Protectant

  • Uses

    helps relieve the local itching and discomfort associated with hemorrhoids

    temporarily shrinks hemorrhoidal tissue and relieves burning

    temporarily provides a coating for relief of anorectal discomforts

    temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

  • Warning

    For external and /or intrarectal use only. Not for oral use.

  • Stop use

    bleeding occurs

    condition worses or does not improve within 7 days

    introduction of applicator into the rectum causes additional pain

  • Warning

    Apply it carfully during pregnancy.

  • Warning

    Keep this and all drugs out of reach of children.

  • Direction

    Apply properly onto anus or apply on affected areas twice a day.

  • Other information

    Store at 20-25 degree Centigrade (68-77 degree Fahrenheit)

  • Inactive ingredients

    Musk Ketone

    Pearl (Hyriopsis Cumming II)

    Borneol

    Sodium Borate

  • Drug Facts

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  • INGREDIENTS AND APPEARANCE
    MAYINGLONG HEMORRHOIDS 
    zinc oxide, petrolatum, lanolin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68511-993
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE800 mg  in 10000 mg
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM7850 mg  in 10000 mg
    Inactive Ingredients
    Ingredient NameStrength
    MUSK KETONE (UNII: 483V3E1L6J)  
    PEARL (HYRIOPSIS CUMINGII) (UNII: A75L5FZ40U)  
    BORNEOL (UNII: M89NIB437X)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68511-993-0110000 mg in 1 CARTON; Type 0: Not a Combination Product10/25/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34612/15/2003
    Labeler - Mayinglong Pharmaceutical Group Co Ltd (526823828)
    Registrant - Mayinglong Pharmaceutical Group Co Ltd (526823828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mayinglong Pharmaceutical Group Co Ltd526823828manufacture(68511-993)
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