Label: ATP HAND SANITIZER MOISTURIZING FORMULA WITH ALOE- alcohol 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 May 25, 2020

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  • ACTIVE INGREDIENT

    Active ingredient(s)                                      Purpose

    Ethyl Alcohol  71%       ...............                 Antiseptic

  • PURPOSE

    • To decrease bacteria on the skin that could cause disease.
    • When water, soap and towel are not available.
    • Recommendd for repeated use.
  • KEEP OUT OF REACH OF CHILDREN

    • Children should be supervised by an adult when using this product.
    • If swallowed, get medical help or contact a Poison Control Center right away.
  • INDICATIONS & USAGE

    • Wet hands thoroughly with product and allow to dry without wiping
    • No rinsing required
    • For Children under 6, use only under adult supervision
    • No recommended for infants.
  • WARNINGS

    For external use only: hands
    Flammable. Keep away from fire or flame.

    When using this product

    • Keep out of eyes, ears, or mouth
    • In case of eye contact, flush eyes thoroughly with water
    • Avoid contact with broken skin
    • Do not inhale or ingest

    Stop use and ask a doctor if 

    • redness or irritation develop 
    • condition persists for more than 72 hours
  • DOSAGE & ADMINISTRATION

    Other information:

    • Store below 105℉(40℃)
    • May discolor certain fabrics
    • Harmful to wood finishes and plastics
  • INACTIVE INGREDIENT

    Water, Glycerin, Aloe Barbadensis gel, carbomer, fragrance

  • PRINCIPAL DISPLAY PANEL

    image of label

  • INGREDIENTS AND APPEARANCE
    ATP HAND SANITIZER MOISTURIZING FORMULA WITH ALOE 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75780-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) alcohol71 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75780-009-01237 mL in 1 BOTTLE; Type 0: Not a Combination Product05/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/25/2020
    Labeler - NINGBO MEINEKE Biotech Technology Co., Ltd. (413126185)
    Establishment
    NameAddressID/FEIBusiness Operations
    NINGBO MEINEKE Biotech Technology Co., Ltd.413126185manufacture(75780-009)
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