Label: STAIN REMOVER (stain remover- bamboo liquid

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

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 28, 2021

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

  • ACTIVE INGREDIENT

    C12-15 PARETH-10 5%

    Sodium dodecyl sulphate 8%

    OCTOXYNOL-11 4%

    Bamboo extract 10.2%

  • INACTIVE INGREDIENT

    Deionized water

    Sodium phosphate, dibasic, dihydrate

    Betaine

    Coconut diethanolamide

  • HOW TO USE

    Step 1-Wipe the fresh stains with a tissue or cloth
    Step 2- Roll the ball until the liquid completely covers the stain
    Step 3- After 10 seconds, gently wipe the stain area witha damp cloth

  • INDICATIONS & USAGE

    Spray enough product where you need to clean up to cover the dirt.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PURPOSE

    In addition to stains

  • STORAGE AND HANDLING

    Keep in a cool and dry place

  • WARNINGS

    1.Do not directly expose the processed stain area to sunlight.
    2.Keep out of reach of children.
    3. If got into eyes, please rinse with plenty of water immediately. Ask doctor for help if necessary.
    4. If swallowed, please go to the hospital immediately and show the doctor product container and label.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    STAIN REMOVER 
    stain remover(bamboo) liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82371-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOXYNOL-11 (UNII: SQL994V0M6) (OCTOXYNOL-11 - UNII:SQL994V0M6) OCTOXYNOL-114 g  in 100 mL
    BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V) (BAMBUSA VULGARIS TOP - UNII:FIW80T6P6V) BAMBUSA VULGARIS TOP10.2 g  in 100 mL
    SODIUM LAURYL SULFATE (UNII: 368GB5141J) (LAURYL SULFATE - UNII:DIQ16UC154) SODIUM LAURYL SULFATE8 g  in 100 mL
    C12-15 PARETH-10 (UNII: Z0QJT9586T) (C12-15 PARETH-10 - UNII:Z0QJT9586T) C12-15 PARETH-105 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)  
    BETAINE (UNII: 3SCV180C9W)  
    WATER (UNII: 059QF0KO0R)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82371-003-018.9 mL in 1 BOTTLE; Type 0: Not a Combination Product12/28/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/28/2021
    Labeler - Zhejiang Dibao Biotechnology Co., Ltd. (603023294)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Dibao Biotechnology Co., Ltd.603023294manufacture(82371-003)