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

  • NDC Code(s): 68511-993-01
  • Packager: Mayinglong Pharmaceutical Group Co Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 20, 2018

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  • Active Ingredients

    Zinc Oxide 0.8g Astrigent

    Petrolatum 7.85g Protectant

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  • Purpose

    Astrigent

    Protectant

    Protectant

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  • 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

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  • Warning

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

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  • Stop use

    bleeding occurs

    condition worses or does not improve within 7 days

    introduction of applicator into the rectum causes additional pain

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  • Warning

    Apply it carfully during pregnancy.

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  • Warning

    Keep this and all drugs out of reach of children.

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  • Direction

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

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  • Other information

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

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  • Inactive ingredients

    Musk Ketone

    Pearl (Hyriopsis Cumming II)

    Borneol

    Sodium Borate

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  • Drug Facts
  • INGREDIENTS AND APPEARANCE
    MAYINGLONG HEMORRHOIDS 
    zinc oxide, petrolatum, lanolin ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68511-993
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 800 mg  in 10000 mg
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 7850 mg  in 10000 mg
    Inactive Ingredients
    Ingredient Name Strength
    MUSK KETONE (UNII: 483V3E1L6J)  
    PEARL (HYRIOPSIS CUMINGII) (UNII: A75L5FZ40U)  
    BORNEOL (UNII: M89NIB437X)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68511-993-01 10000 mg in 1 CARTON; Type 0: Not a Combination Product 10/25/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part346 12/15/2003
    Labeler - Mayinglong Pharmaceutical Group Co Ltd (526823828)
    Registrant - Mayinglong Pharmaceutical Group Co Ltd (526823828)
    Establishment
    Name Address ID/FEI Business Operations
    Mayinglong Pharmaceutical Group Co Ltd 526823828 manufacture(68511-993)
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