Label: 100% PURE HAND SANITIZER HYDRATING- ethyl alcohol gel

  • NDC Code(s): 52667-011-01, 52667-011-02
  • Packager: Purity Cosmetics
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 19, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    For cleaning hands when water is not available to help reduce bacteria on the skin. Recommended for repeated use.

  • Warnings:

    • ​For external use only.
  • STORAGE AND HANDLING

    • Flammable, keep away from fire, sparks, and sources of ignition.
    • Do not store above 104°F/40°C.
  • WHEN USING

    • When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children. ​If swallowed, get medical help or contact a Poison Control Center immediately.
  • OTHER SAFETY INFORMATION

    • Avoid contact with broken skin.
  • STOP USE

    • Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.
  • Directions:

    Dispense directly on hands and rub in thoroughly. For children under 6, use adult supervision. Not recommended for infants.

  • Other Ingredients:

    Aloe Barbadensis (Aloe Vera) Leaf Juice*, Glycerin, Hydroxypropyl Guar, Citric Acid, Aqua (Water) *Organic Ingredient

  • Questions or Comments?

    Call 1.415.814.9788 or visit www.100PercentPure.com

  • PRINCIPAL DISPLAY PANEL

    100% Pure Hand Sanitizer Hydrating Gel

    Product NDC 52667-011 Label

  • INGREDIENTS AND APPEARANCE
    100% PURE HAND SANITIZER  HYDRATING
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52667-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52667-011-0150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/03/202002/09/2025
    2NDC:52667-011-02473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/03/202002/09/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/03/202002/09/2025
    Labeler - Purity Cosmetics (055795259)
    Registrant - Our Babylon LLC (105266218)
    Establishment
    NameAddressID/FEIBusiness Operations
    Our Babylon LLC105266218manufacture(52667-011)