Label: LEGERE BAMBOO FOOT PATCH- topical starch patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 29, 2022

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  • PURPOSE

    Skin Protectant

  • Uses

    May help relieve minor aches and pain

  • Active Ingredient

    Topical Starch 32.33%

  • Warnings

    For external use only / Don’t eat or swallow it

  • Warnings

    Keep out of the reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • When using this product

    ■ Do not use otherwise than directed.

    ■ Do not stretch out the adhesive tape.

    ■ Do not take out the contents from the patch.

    ■ If the patch has been ripped, discard it immediately.

  • Stop use and ask a doctor if

    ■ If allergic reaction or irritation occurs

    ■ If you are pregnant, nursing or under medial treatment

  • Warnings

    ■ On wounds, damaged skin, or face.

    ■ If you are allergic to any ingredients of this product.

    ■ With, or at the same time as, other external products.

  • Inactive Ingredients

    Bamboo vinegar, Tourmaline, Eucalyptus oil, Mugwort extract, Loquat extract, Vitamin C, Highly purified silica, Perlite, Polyhydric alcohol

  • directions

    Adults and children 4 years of age and over:

    Step 1: Clean and dry area for the patch to be attached.

    Step 2: Remove the protective cover sheet and gently apply.

    Step 3: Leave it on at least 4hours before remove.

    Children under 4years of age: Consult with a doctor.

  • Légère Bamboo Foot Patch

    82504-102-01

    label

  • INGREDIENTS AND APPEARANCE
    LEGERE BAMBOO FOOT PATCH 
    topical starch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82504-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STARCH, CORN (UNII: O8232NY3SJ) (STARCH, CORN - UNII:O8232NY3SJ) STARCH, CORN32.33 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PHYLLOSTACHYS EDULIS VINEGAR (UNII: MR94DK8ZSM)  
    PERLITE (UNII: 0SG101ZGK9)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    POLIGLUSAM (UNII: 82LKS4QV2Y)  
    ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)  
    ERIOBOTRYA JAPONICA LEAF (UNII: Z02066SV11)  
    GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)  
    SCHORL TOURMALINE (UNII: 173O8XLY6T)  
    SORBITOL (UNII: 506T60A25R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82504-102-0140 g in 1 BOX; Type 0: Not a Combination Product01/10/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/10/2022
    Labeler - Myriad Co., Ltd. (695004202)
    Registrant - Myriad Co., Ltd. (695004202)
    Establishment
    NameAddressID/FEIBusiness Operations
    Myriad Co., Ltd.695004202manufacture(82504-102)
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