Label: ANTI-BACTERIAL STICKER patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 October 5, 2020

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

  • Active Ingredient(s)

    Peppermint Oil 0.25%

  • Purpose

    Skin Protectant

  • Use

    Temporarily lower the microbes in the surrounding environment, allergies, nose irritation

  • Warnings

    For external use only. It’s a normal phenomenon to generate heat when the essential oil is active.

  • WHEN USING

    Please stick the sticker on the lower corner of the garment or thicker part of the garment.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.In case of consumption or allergies get medical help right away.

  • Directions

    Adults and children over 3 years attach 1 piece every 4 to 6 hours

    Children under 3 years ask a doctor if there are allergies.

  • Other information

    Storage Keep in dry and cool (under 25˚C) place and away from direct sunlight

  • Inactive ingredients

    Polypropylene film, Art Paper, Glassine Release Paper, Acrylic Resin

  • Package Label - Principal Display Panel

    Front and Back Labels10 patches, NDC: 80745-001-01

  • INGREDIENTS AND APPEARANCE
    ANTI-BACTERIAL STICKER 
    anti-bacterial sticker patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80745-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PEPPERMINT OIL (UNII: AV092KU4JH) (PEPPERMINT - UNII:V95R5KMY2B) PEPPERMINT OIL0.25 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYPROPYLENE (30000 MW) (UNII: T71QXI2O62)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80745-001-0110 in 1 PACKAGE10/05/2020
    110 mg in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35610/05/2020
    Labeler - YCM PRODUCTS CO., LTD (656858839)
    Establishment
    NameAddressID/FEIBusiness Operations
    YCM PRODUCTS CO., LTD656858839manufacture(80745-001)