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Eczemin (Alva-Amco Pharmacal Companies, Inc.)

Available Formats

Dosage Form Package Information Links
CREAM 1 JAR in 1 CARTON (52389-628-04) > 113 g in 1 JAR Label Information

Complete Eczemin Information

  • Active ingredient

    Pramoxine hydrochloride, 1%


  • Purpose

    Topical analgesic


  • Uses

    For the temporary relief of itching skin.


  • Warnings

    For external use only

    When using this product avoid contact with the eyes.

    Stop use and ask a doctor if

    • Condition worsens
    • symptoms persist for more than 7 days
    • symptoms clear up and occur again within a few days

    Keep out of reach of children.  If swallowed, get medical help or contact a poison control center right away.


  • Directions

    Read all directions and warnings before use. Use only as directed. Apply to affected area not more than 3 to 4 times daily. Intended for use by normally healthy adults only. Persons under 18 years of age or those with highly sensitive or allergic skin should use only as directed by a doctor.


  • Other information

    You may report serious side effects to the phone number provided under Questions? below.


  • Inactive ingredients

    Ceteareth-6, ceteareth-25, cetostearyl alcohol, diazolidinyl urea, iodopropynyl butylcarbamate, mineral oil, purified water, stearyl alcohol.


  • Questions?

    1-800-792-2582


  • INGREDIENTS AND APPEARANCE
    ECZEMIN 
    pramoxine hydrochloride cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:52389-628
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Pramoxine hydrochloride (UNII: 88AYB867L5) (Pramoxine - UNII:068X84E056) Pramoxine hydrochloride 10 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    Cetostearyl alcohol (UNII: 2DMT128M1S)  
    Diazolidinyl urea (UNII: H5RIZ3MPW4)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Mineral oil (UNII: T5L8T28FGP)  
    Water (UNII: 059QF0KO0R)  
    Stearyl alcohol (UNII: 2KR89I4H1Y)  
    Ceteareth-25 (UNII: 8FA93U5T67)  
    CETEARETH-6 (UNII: 2RJS3559D3)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52389-628-04 1 in 1 CARTON
    1 113 g in 1 JAR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 11/16/2011
    Labeler - Alva-Amco Pharmacal Companies, Inc. (042074856)