Label: ALL HEALTH ALLIANCE HAND SANITIZER WITH ALOE AND VITAMIN E 400ML- alcohol liquid

  • NDC Code(s): 54860-151-01
  • Packager: Shenzhen Lantern Scicence Co Ltd
  • 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 March 26, 2020

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

  • Drug Facts

    all health alliance hand sanitizer with aloe and vitamin E 400ml

  • Medicical Ingredient

    Medicical Ingredient Purpose

    Ethyl Alcohol 75%(V/V) Antiseptic

  • Features

    To decrease bacteria on the skin that could cause disease.

    Recommended for repeated use.

    use anywhere without water.

  • Warning

    For external use only.

    Flammable, keep away from heat and flame.

    Discontinue if skin becomes irritated and ask a doctor .

    Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poson control center immediately.

  • Non-Medicinal

    Water, Glycerin,Aloe Yohjyu Mastu Ekisu,Tocopheryl Acetate,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Aminomethyl propanol,Parfum.

  • Directions

    Wet hands thoroughly with product and rub until dry without wiping

    For children under 6, use only under adult supervision.

    Not recommended for infants.

    When using this product

    keep out of eyes. In case of contact with eyes, flush thoroughly with water.

    Do not inhale or ingest.

    Avoid contact with broken skin.

    Other information

    Do not store above 105F.

    May discolor some fabrics.

    Harmful to wood finishes and plastics.

  • PRINCIPAL DISPLAY PANEL

    all health alliance hand sanitizer 400ml

  • INGREDIENTS AND APPEARANCE
    ALL HEALTH ALLIANCE HAND SANITIZER WITH ALOE AND VITAMIN E 400ML 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-151
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 940 (UNII: 4Q93RCW27E) 0.3 g  in 100 g
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.1 g  in 100 g
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.1 g  in 100 g
    ALOE (UNII: V5VD430YW9) 0.15 g  in 100 g
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.09 g  in 100 g
    WATER (UNII: 059QF0KO0R) 28.388 g  in 100 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 g  in 100 g
    Product Characteristics
    Colorwhite (transparant) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54860-151-01400 g in 1 BOX; Type 0: Not a Combination Product03/26/2020
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/26/2020
    Labeler - Shenzhen Lantern Scicence Co Ltd (421222423)
    Registrant - Lantern Beauty America,INC. (117371139)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern cosmetic Co Ltd421222423manufacture(54860-151)