Label: HAND SANITIZER WITH ALOE VERA- alcohol gel

  • NDC Code(s): 58400-010-01, 58400-010-02, 58400-010-04, 58400-010-08, view more
    58400-010-30, 58400-010-55
  • Packager: Pharmco Laboratories, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Uses

    Hand sanitizer to help reduce bacteria on the skin

  • Warnings

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

    Do not use

    • in children less that 2 months of age
    • on open wounds

    When using this product, keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Discontinue use if irritation or redness develops.

    If condition persists for more than 72 hours, consult a doctor.

    Keep out of reach of children. If swallowed get medical help or call a poison control center immediately.

  • Directions

    • Place enough product in your palm 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

    • Store below 43°C (110°F)
    • May discolor certain fabrics or surfaces.
  • Inactive Ingredients

    Water, Glycerin, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Citric Acid, Sodium Hydroxide

  • SPL UNCLASSIFIED SECTION

    Manufactured by:
    Pharmco Laboratories, Inc.
    3520 South St. Titusville, FL 32780

  • PRINCIPAL DISPLAY PANEL - 59 mL Tube Label

    pharmco
    MANUFACTURER OF PREMIUM SKIN CARE PRODUCTS

    HAND
    SANITIZER
    with aloe vera

    2 fl oz. (59 mL)

    PRINCIPAL DISPLAY PANEL - 59 mL Tube Label
  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER WITH ALOE VERA 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58400-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58400-010-0259 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2020
    2NDC:58400-010-04125 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    3NDC:58400-010-08228 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2020
    4NDC:58400-010-30885 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    5NDC:58400-010-013780 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    6NDC:58400-010-55207000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00305/01/2020
    Labeler - Pharmco Laboratories, Inc. (096270814)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharmco Laboratories, Inc.096270814MANUFACTURE(58400-010) , LABEL(58400-010) , PACK(58400-010)
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