Label: BODY BLENDS VANILLA SUGAR ANTI-BACTERIAL HAND SANITIZER- alcohol liquid

  • 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 July 5, 2010

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  • ACTIVE INGREDIENT

    Active ingredients                                               Purpose

    Ethyl Alcohol 62%                                               Antiseptic

  • DESCRIPTION

    Uses   Reduce bacteria on hands that can cause disease

  • WARNINGS

    Warnings

    For external use only

    Flammable: Keep away from fire or flame

    When using this product，avoid contact with eyes. If contact occurs, flush with water

    Stop using and ask a doctor, if irritation or rash persists

    Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center immediately. 

  • WHEN USING

    Directions   

    Rub a small amount into hands until dry


  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Propylene Glycol,  PEG-40 Hydrogenated Castor Oil, Fragrance, Carbomer, Triethanolamine, Lactose, Cellulose, Hydroxypropyl Methylcellulose, Jojoba Ester, Tocopheryl Acetate, Ascorbyl Palmitate, Disodium EDTA, FD and C red No. 4, FD and C Yellow No. 5

  • PRINCIPAL DISPLAY PANEL

    lablabel

  • INGREDIENTS AND APPEARANCE
    BODY BLENDS VANILLA SUGAR ANTI-BACTERIAL HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49981-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62.00 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 34.04989 g  in 100 g
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 1.8 g  in 100 g
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) 1.0 g  in 100 g
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) 0.29 g  in 100 g
    TROLAMINE (UNII: 9O3K93S3TK) 0.28 g  in 100 g
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) 0.01 g  in 100 g
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) 0.01 g  in 100 g
    EDETATE DISODIUM (UNII: 7FLD91C86K) 0.03 g  in 100 g
    FD&C RED NO. 4 (UNII: X3W0AM1JLX) 0.00003 g  in 100 g
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.00008 g  in 100 g
    HYPROMELLOSE 2208 (15000 CPS) (UNII: Z78RG6M2N2) 0.01 g  in 100 g
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.01 g  in 100 g
    ASCORBYL PALMITATE (UNII: QN83US2B0N) 0.01 g  in 100 g
    VANILLA (UNII: Q74T35078H) 0.5 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49981-021-0159 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33307/10/2010
    Labeler - Xiamen Anna Global Co., Ltd (527060704)
    Registrant - Xiamen Anna Global Co., Ltd (527060704)
    Establishment
    NameAddressID/FEIBusiness Operations
    Xiamen Anna Global Co., Ltd527060704manufacture
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