Label: STRIDEX NATURALLY CLEAR liquid

  • Category: HUMAN OTC DRUG LABEL

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 November 23, 2009

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  • ACTIVE INGREDIENT

     SALICYLIC ACID 1% WITH ACNE MEDICATION


  • PURPOSE


    Acne medication



    • For the treatment and management of acne
    • reduces the number of acne pimples and blackheads and allows the skin to heal
    • helps to prevent new acne pimples from forming












  • WHEN USING


    FOR EXTERNAL USE ONLY

    Allergy alert:

    do not use this product it you have a known allergy to salicylic acid.



    • Cleanse the skin thoroughly before applying medication
    • use the pad to wipe the entire affected area
    • repeat with a clean pad as necessary to remove remaining traces of dirt,because excessive drying of the skin may occur , start with one application
                   daily , then gradually increase to two to three times daily as needed or as directed by a doctor
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day
    • do not leave pad on skin for an extended period of time
    • keep away from eyes ,lips and other mucous membrane

    using other topical acne medications at the same time or immediately following use of this product may increase
    dryness or irritation of the skin. If this occurs , only one medication should be used unless directed by doctor.


    If swallowed get get medical help or contact a posion control center right away.
  • PRINCIPAL DISPLAY PANEL



    Naturally Clear

    Stridex
    Stridex label


    The Natural acne solution with the proven effectiveness of stridex












  • INGREDIENTS AND APPEARANCE
    STRIDEX  NATURALLY CLEAR
    stridex naturally clear liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10157-1070
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (BENZOIC ACID - UNII:8SKN0B0MIM) SALICYLIC ACID0.1 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10157-1070-170 in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33311/23/2009
    Labeler - Blistex inc (005126354)
    Establishment
    NameAddressID/FEIBusiness Operations
    Blistex Inc005126354manufacture
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