Label: SUN BUM 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 February 4, 2022

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  • Drug Facts

  • Active ingredient

    Ethyl alcohol 62%

    Purpose

    Antiseptic

  • Uses

    to help reduce bacteria on the skin

    recommended for repeated use

  • Warnings

    For external use only

    Flammable keep away from fire or flame

    When using this product

    do not use in or near the eyes. In case of eye contact, rinse thoroughly with water.

    Stop use and ask a doctor if 

    irritation or rash appears and lasts. Condition persists for more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • spray enough product in your palms to thoroughly cover your hands 
    • rub hands together briskly until dry
    • children under 6 years of age should be supervised when using this product
  • Other information

    • do not store above 104° F/40°C
    • may discolor some fabrics or surfaces
  • Inactive ingredients

    water,fragrance,glycerin,aloe barbadensis leaf juice, cucumis sativus (cucumber) fruit extract, musa sapientum (banana) fruit extract, hedychium coronarium root extract, gardenia taitensis flower extract, cocos nucifera (coconut) oil, sea salt, ethylhexylglycerin

  • Questions?

    1-877-978-6286

  • Package Labeling:

    Bottle5

  • INGREDIENTS AND APPEARANCE
    SUN BUM HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69039-615
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CUCUMBER (UNII: YY7C30VXJT)  
    BANANA (UNII: 4AJZ4765R9)  
    HEDYCHIUM CORONARIUM ROOT (UNII: 92A6N0IQN9)  
    GARDENIA TAITENSIS FLOWER (UNII: T0OCU8201Y)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    SEA SALT (UNII: 87GE52P74G)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69039-615-0159 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/01/2020
    Labeler - Sun Bum LLC (028642574)
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