Label: RAPIDOL HEMORRHOIDAL- glycerin, phenylephrine hcl, pramoxine hcl, white petrolatum cream

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated August 30, 2024

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  • Drug Facts

  • Active ingredients & Purposes

    Active ingredients

    Purposes

    Glycerin 14.4%...........................

    		Protectant
    Phenylephrine HCl 0.25%..........Vasoconstrictor
    Pramoxine HCl 1 %....................Local anesthetic
    White petrolatum 15%................Protectant

  • Uses

    • for the temporary relief of local itching and discomfort associated with
    • hemorrhoid
    • anorectal inflammation
    • temporarily shrinks hemorrhoidal tissue
    • temporarily relieves the symptoms of perianal skin irritation
  • Warnings

    FOR EXTERNAL 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 the prostate gland

    Ask a doctor of 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
    • do not put this product into the rectum by using fingers or any mechanical device or applicator

    Stop use and consult a doctor if

    • condition worsens or does not improve within 7 days
    • bleeding occurs

    If pregnant or breastfeeding,

    ask a doctor before use.

    KEEP OUT OF THE REACH OF CHILDREN.

    In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

  • Directions

    • adults: when practical, cleanse the affected area with 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

    apply externally to the affected area after a bowel movement, no more than 4 times daily

    • children under 12 years of age: consult a doctor
  • Other information

    • store between 60-77°F (20-25°C)
    • do not use if foil seal under cap is broken or missing
  • Inactive Ingredients

    aloe vera leaf, alpha tocopherol (Vit. E), butylated hydroxyanisole, carboxymethylcellulose sodium, cetostearyl alcohol, cetyl alcohol, citric acid monohydrate, edetate disodium, glyceryl monostearate, methylparaben, mineral oil, panthenol, propylparaben, sodium benzoate, steareth-20, xanthan gum, water

  • Questions?​

    +1-866-359-3478 (M-F) 9AM to 5 PM EST or www.pharmadel.com

    Distributed by/ Distribuido por:

    Pharmadel LLC

    New Castle, DE 19720

    Made in India/ Hecho en India

  • Product Labeling

    pdp rapidol Hemorrhoids

  • INGREDIENTS AND APPEARANCE
    RAPIDOL HEMORRHOIDAL 
    glycerin, phenylephrine hcl, pramoxine hcl, white petrolatum cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55758-448
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN14.4 g  in 100 g
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE0.25 g  in 100 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE1 g  in 100 g
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55758-448-011 in 1 CARTON08/30/2024
    130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01508/30/2024
    Labeler - Pharmadel LLC (030129680)
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