Label: ANTIOCHPHARMA RAPIDGEL HAND SANITIZER- alcohol gel

  • NDC Code(s): 11383-309-02, 11383-309-09, 11383-309-12, 11383-309-34
  • Packager: Weeks & Leo
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Alcohol 70% v/v..................................................................Antiseptic

  • Purpose

    Antiseptic

  • Uses

    hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only

    Do not use

    in children less than 2 months of ageon open skin wounds

    When using this product

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

    Stop use and ask a doctor if

    Irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children

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

  • Directions

    Place enough product on hands to cover all surfaces. Rub hands together until dry.

    Supervise children under 6 years of age when using this product to avoid swallowing

  • Other Information

    Store between 15–30 °C (59–86 °F)

    Avoid freezing and excessive heat above 40 °C (104 °F)

    Close cap after use

    May discolor certain fabrics or surfaces

  • Inactive Ingredients

    acrylates/C10–30 alkyl acrylate crosspolymer, aminomethyl propanol, glycerin, isopropyl myristate, propylene glycol, purified water, SD alcohol 40-B, tocopheryl acetate

  • Package Label

    AntiochPharma

    Hand Sanitizer

    With Vitamin E and Moisturizers

    Kills 99.99 %of germs

    made in USA

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    ANTIOCHPHARMA RAPIDGEL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11383-309
    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)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    RAPIDGEL EZ1 (UNII: 33JH4A7R2K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11383-309-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product03/24/2020
    2NDC:11383-309-34100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/24/2020
    3NDC:11383-309-09259 mL in 1 BOTTLE; Type 0: Not a Combination Product03/24/2020
    4NDC:11383-309-0259 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/24/2020
    Labeler - Weeks & Leo (005290028)
    Registrant - Weeks & Leo Co., Inc. (005290028)
    Establishment
    NameAddressID/FEIBusiness Operations
    Weeks & Leo Co., Inc.005290028manufacture(11383-309)