Label: ALTRA FOAMING HAND SANITIZER WITH ALOE AND VITAMIN E- alcohol solution

  • NDC Code(s): 30805-012-04, 30805-012-05, 30805-012-07, 30805-012-09
  • Packager: Buckeye International, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 April 5, 2020

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  • Active ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antibacterial

  • Uses

    • Hand sanitizer to help reduce bacteria on the skin that could cause disease
    • Recommended for repeated use
  • Warnings

    Flammable, Keep away from fire or flame.

    For external use only.

    When using this product do not use in or near eyes.

    If in eyes, flush thoroughly with water.

    If irritation or rash appears and persists, stop use and see a physician.

    Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately

  • Directions

    • Dispense an adequate amount of hand sanitizer
    • Rub hands together until completely dry
  • Other information

    • Do not store above 110 F (43 C)
    • May discolor some fabrics or surfaces
  • Inactive ingredients

    Water (Aqua), PEG-10 Dimethicone, PEG-12 Dimethicone, PEG-8 Dimethicone, Glycerine, Propylene Glycol, Isopropyl Myristate, Fragrance (parfum), Aloe Barbadesis Leaf Juice and Tocopheryl Acetate.

  • Questions?

    Call Buckeye International, Inc. 314-291-1900

    Monday through Friday 8:00 a.m. to 5:00p.m. CST

  • PRINCIPAL DISPLAY PANEL

    ALTRA

    Foaming Hand

    Sanitizer

    with Aloe and Vitamin E

    Hand Hygiene

    Manufacteyred By

    Buckeye International

    2700 Wagner Place Maryland Heights

    MO 63043 USA (314) 291-1900

    Product # 71051120

    Net Contents 1200 mL (40.6 fl oz)

    container label

  • INGREDIENTS AND APPEARANCE
    ALTRA FOAMING HAND SANITIZER WITH ALOE AND VITAMIN E 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30805-012
    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
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30805-012-041200 mL in 1 BAG; Type 0: Not a Combination Product04/05/2020
    2NDC:30805-012-0550 mL in 1 BOTTLE; Type 0: Not a Combination Product04/05/2020
    3NDC:30805-012-07550 mL in 1 BOTTLE; Type 0: Not a Combination Product04/05/2020
    4NDC:30805-012-091000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/05/2020
    Labeler - Buckeye International, Inc. (077132280)
    Establishment
    NameAddressID/FEIBusiness Operations
    Buckeye International, Inc.077132280manufacture(30805-012)
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