Label: HAND SANITIZING WITH LAVENDER OIL- alcohol gel

  • NDC Code(s): 59088-413-06, 59088-413-08, 59088-413-14, 59088-413-31, view more
    59088-413-36, 59088-413-39
  • Packager: PureTek Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 1, 2024

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  • Active Ingredient

    Alcohol 62% (v/v)

  • Purpose

    Anti-Bacterial

  • Uses

    ■ Hand sanitizer to help reduce bacteria on the skin

  • Warnings

    ■ Flammable. Keep away from fire or flame.

  • When using this product

    ■ do not use in or near eyes. In case of contact, rinse eyes throughly with water

  • Stop use and ask a doctor if

    ■ irritation or redness develop and last 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

    ■ Dispense and rub onto hands until dry. Do not rinse off.

    ■ Children under 6 years of age should use this product under supervision.

    ■ repeat as necessary

  • Other information

    ■ Do not store above 110°F (43°C)

  • Inactive ingredients

    Aloe Barbadensis (aloe vera) Leaf Juice, Butyrospermum Parkii (Shea) Butter, Glycerin, Lavandula Angustifolia (Lavender) Oil, Panthenol, Polyacrylate Crosspolymer-6, Water (Aqua)

  • GenRx Hand Sanitizing Gel with Lavender

    Manufactured in the USA by PureTek Corporation
    Panorama City, CA 91402 USA
    877-921-7873
    www.genrxwoundcare.com

    List No:41431JLA

    NDC 59088-413-08

    4 floz Label

    NDC 59088-413-31

    16.9 floz

    NDC 59088-413-39

    24 FLOZ

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZING WITH LAVENDER OIL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59088-413
    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)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    WATER (UNII: 059QF0KO0R)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C)  
    LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59088-413-061 in 1 KIT06/05/2020
    1NDC:59088-413-39710 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:59088-413-361 in 1 KIT06/05/2020
    2NDC:59088-413-141 in 1 KIT
    2NDC:59088-413-08118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:59088-413-31500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01406/05/2020
    Labeler - PureTek Corporation (785961046)
    Establishment
    NameAddressID/FEIBusiness Operations
    PureTek Corporation785961046manufacture(59088-413) , label(59088-413)
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