Label: HAND SANITIZER- alcohol cloth

  • 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 June 23, 2020

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

  • Active Ingredient(s)

    Belzalkonium chloride 0.12 % w/w. Purpose: Antiseptic

    Polyaminopropyl Biguanide 0.5% w/w Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    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. Flammable. Keep away from heat or flame

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    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.

  • STOP USE

    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

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

    Water, glycerin, disodium cocoamphodiacetate, polysorbate 20, decyl glucoside, iodopropynyl butyñcarmate, methylisothiazolinone, PEF- 12 dimethicone, fragrance, aleo vera and citric acid.

  • Package Label - Principal Display Panel

    PDP 150 g NDC: 77824-002-02 PDP 150 gPI 150 g NDC: 77824-002-02 PI 150 g

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77824-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.12 g  in 100 mL
    POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET) (POLYAMINOPROPYL BIGUANIDE - UNII:DT9D8Z79ET) POLYAMINOPROPYL BIGUANIDE0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE PEG-7 PANTHENYL PHOSPHATE (12 PANTHENOL) (UNII: 7MA9F33W92) 0.12 mL  in 100 mL
    ABRONIA FRAGRANS FLOWER (UNII: XAV1S68QBA) 0.1 mL  in 100 mL
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) 0.17 mL  in 100 mL
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y) 0.2 mL  in 100 mL
    ALOE VERA FLOWER (UNII: 575DY8C1ER) 0.08 mL  in 100 mL
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 0.04 mL  in 100 mL
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) 0.17 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 1 mL  in 100 mL
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) 0.6 mL  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH) 0.2 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77824-003-01150 mL in 1 POUCH; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/30/2020
    Labeler - Betone, S.A de C.V. (813262755)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betone, S.A de C.V.813262755manufacture(77824-003) , pack(77824-003) , label(77824-003)