Label: ALOBON SANITIZERSPRAY- sanitizer spray spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 August 18, 2020

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  • Active Ingredient

    Alcohol 75%

  • Purpose

    Antiseptic

  • Use

    For decreasing bacteria on the skin

  • Warnings

    • For external use only
    • Flammable, keep away from fire and flame
    • Dose not contain grain alcohol; do not drink. If taken internally will produce serious gastric disturbances.

    When using this product

    When using this product

    • Aviod the eyes and mucous membrances
    • In the case of eyes and mucous membrances contact, rinse area thoroughly with water

    Stop use and ask a doctor if

    Stop use and ask a doctor if

    • Condition worsens
    • Redness or irritation develops
    • If condition persists for more than 3 days

    Keep out of reach of children

    Keep out of reach of children

    If swallowed contact a doctor or Poison Control Center immediately.

  • Directions

    • Place enough Product in your palm to cover hands and rub hands together briskyly until dry.
    • Supervise children in the use of this product.
    • In the case of eye contact, rinse eyes thoroughly with water.
  • Other information

    • Store between 15-30°C (59-86F).
    • Avoid freezing and excessive heat above 40°C (104F).
  • Inactive ingredients

    Ammonium acryloyldimethyltaurate/vp copolymer, chloroxylenol, glycerin, methyl gluceth-10, water.

  • Package Label/Principal Display Panel

    NDC 78692-613-34; 100 mL

    ALOBON Sanitizer Spray

  • INGREDIENTS AND APPEARANCE
    ALOBON SANITIZERSPRAY 
    sanitizer spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78692-613
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    METHYL GLUCETH-10 (UNII: N0MWT4C7WH)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    CHLOROXYLENOL (UNII: 0F32U78V2Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78692-613-34100 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/01/2020
    Labeler - Shantou Wanbang Cosmetic Co., Ltd. (552659581)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shantou Wanbang Cosmetic Co., Ltd.552659581manufacture(78692-613)
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