Label: APOLLO INSTANT HAND SANITIZER- instant 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 8, 2021

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  • Active ingredient

    Alcohol 75%

  • Purpose

    Antiseptic

  • Uses:

    Hand sanitizer to help decrease bacterial on the skin, when water, soap& towel are not available. Recommended for repeated use.

  • Warnings

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

    Do not apply around eyes. Do not use in ears & mouth.

  • WHEN USING

    When using this product,

    Avoid contact with eyes. In case of contact flush eyes with water.

  • STOP USE

    Stop use and ask a doctor

    If redness or irritation develop and persist for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    Children must be supervised in use of this product.

  • Directions

    Place enough product into your palms and thoroughly spread on both hands. Rub into skin until dry.

  • Other information

    Store below 110℉（43℃）

    May discolor certain fabrics or surfaces.

  • Inactive ingredients

    Water, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aminomethyl Propanol, Propylene Glycol, Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Power, Lactic Acid, Citric Acid.

  • PDP

    3785ml NDC: 74658-009-01

    3785ML Label

  • INGREDIENTS AND APPEARANCE
    APOLLO INSTANT HAND SANITIZER 
    instant hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78303-002
    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
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    3-HEXENYL ACETATE, (3Z)- (UNII: 6INA6GC5I6)  
    3-HEXEN-1-OL, (3Z)- (UNII: V14F8G75P4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    NEROL (UNII: 38G5P53250)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    CYCLAMEN ALDEHYDE (UNII: 4U37UX0E1E)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78303-002-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/02/2020
    Labeler - Sbu Group L.P. (841530095)
    Registrant - GUANGZHOU XUELEI COSMETIC CO.,LTD. (526885026)
    Establishment
    NameAddressID/FEIBusiness Operations
    GUANGZHOU XUELEI COSMETIC CO.,LTD.526885026manufacture(78303-002) , pack(78303-002) , label(78303-002)
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