Label: HEMORRHOIDAL PAIN RELIEF- hemorrhoidal pain relief ointment ointment

  • NDC Code(s): 13709-334-01
  • Packager: Neilmed Pharmaceuticals Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 11, 2025

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

  • Drug Facts

    Active Ingredients:

    Mineral Oil 14%

    Petrolatum 74.9%

    Phenylephrine HCl 0.25%

  • Drug Facts:

    Purpose

    Protectant

    Protectant

    Vasoconstrictor

  • 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
  • Warnings:

    For external and/or intrarectal use only

  • Ask a doctor before use if you have:

    • Heart disease
    • High blood pressure
    • Thyroid disease
    • Diabetes
    • Difficulty in urination due to enlargement of prostate gland
  • Ask a doctor or pharmacist before use if you are:

    Presently taking a prescription drug for high blood pressure or depression

  • When using this product:

    • Do not exceed the recommended daily dosage unless directed by a doctor
  • Stop use and ask doctor if:

    • Bleeding occurs
    • Condition worsens or does not improve within 7 days
    • Introduction of applicator into the rectum causes additional pain
  • If pregnant or breast-feeding:

    Ask a health professional before use.

  • Keep out of reach of children.

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

  • Directions:

    • Adults: When practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before applying ointment.
    • When first opening the tube, puncture foil seal with top end of cap.
    • Apply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement.
    • Intrarectal use: Remove cover from the applicator, attach applicator to tube, lubricate applicator well and gently insert applicator into the rectum, thoroughly cleanse applicator after each use and replace cover.
    • Also apply ointment to external area.
    • Regular use provides continual therapy for relief of symptoms.
  • Other Information:

    Store at 15°C – 30°C (59°F – 86°F)

    • Children under 12 years of age: ask a doctor
  • Inactive ingredients:

    Benzoic acid, butylated hydroxytoluene, corn oil, glycerin, lanolin, lanolin alcohol, methylparaben, propylparaben, paraffin wax, purified water, thymus vulgaris oil, tocopherol, acetate, white wax

  • Questions or comments?

    1 (877) 477-8633

    TAMPER EVIDENT: DO NOT USE IF SEAL ON TUBE IS PUNCTURED OR MISSING

  • Important:

    Please do not discard this printed box and any enclosed printed material. The inside final product may not have all the details you require for the ongoing use of the product.

  • PRINCIPAL DISPLAY PANEL

    Hemorrhoidal Ointment

  • INGREDIENTS AND APPEARANCE
    HEMORRHOIDAL PAIN RELIEF 
    hemorrhoidal pain relief ointment ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13709-334
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM749 mg  in 1 g
    MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL140 mg  in 1 g
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE2.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    WATER (UNII: 059QF0KO0R)  
    THYMUS VULGARIS (THYME) OIL (UNII: 2UK410MY6B)  
    LANOLIN (UNII: 7EV65EAW6H)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    LANOLIN ALCOHOL (UNII: 884C3FA9HE)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    CORN OIL (UNII: 8470G57WFM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13709-334-011 in 1 CARTON06/11/2025
    157 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01506/11/2025
    Labeler - Neilmed Pharmaceuticals Inc. (799295915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Neilmed Pharmaceuticals Inc.799295915manufacture(13709-334)