Label: ADVANCED HAND SANITIZER gel

  • 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 November 22, 2020

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  • Active Ingredient

    Alcohol 75%

  • Purpose

    /

  • Uses

    Use WBM Care Hand Sanitizer anytime and anywhere.

  • Warnings

    /

  • DO NOT USE

    Don't Use If You Are Allergic To Alcohol. Avoid Fire And Don't Use Near Any Flame. Please Keep In Dry And Cool Place. Long-time Storage May Cause Precipitation Due To Plants Extract. Safe To Use. Avoid Contact With Eyes, Mouth And Wounds. Please Seek For Medical Help If Irritation Occurs.

  • WHEN USING

    Great alternative when soap and water are not available.
    Just apply on hands and gently massage. Easy to clean and protect your hands for whole day.
    WBM Care Hand Sanitizer fit a variety of in-home, Office placement locations, Schools, Cars and everywhere

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

    /

  • Directions

    /

  • Other information

    /

  • Inactive ingredients

    AQUA,SODIUM, CARBOMER,ALOE BARBADENSIS LEAF EXTRACT, BETAINE

  • Package Label - Principal Display Panel

    100

  • INGREDIENTS AND APPEARANCE
    ADVANCED HAND SANITIZER 
    advanced hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43116-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BETAINE (UNII: 3SCV180C9W)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM (UNII: 9NEZ333N27)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43116-007-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/31/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/31/2020
    Labeler - Shenzhen Shierjie Biological Engineering Co., LTD (547610261)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Shierjie Biological Engineering Co., LTD547610261manufacture(43116-007)
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