Label: EVERYDAY EVERYWHERE HAND SANITIZER- alcohol gel

  • 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 May 8, 2020

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  • ACTIVE INGREDIENT

    Active ingredients: Ethyl alcohol 70.0%

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Polysorbate 80, Aloe barbadensis leaf extract, Fragrance

  • PURPOSE

    Purpose: Antiseptic

  • WARNINGS

    Warnings:

    For external use only : Hand
    Flammable, keep away from fire or flame.
    When using this product
    ■ keep out of eyes. In case of contact with eyes, rinse eyes thoroughly with water.
    Stop immediately and consult a doctor if you experience
    ■ irritation or rash appears and lasts

  • 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.

  • Uses

    Uses:

    ■ to decrease bacteria on the skin that could cause disease
    ■ recommended for repeated use

  • Directions

    Directions:

    ■ put enough product in your palm to cover hands and rub hands together briskly until dry.
    ■ for children under 6, use only under adult supervision
    ■ not recommended for infants

  • Other Information

    Other Information

    - do not store above 86℉(30℃)
    - may discolor some fabrics

  • PACKAGE LABEL : EVERYDAY EVERYWHERE HAND SANITIZER GEL 60mL

    Image of carton

  • PACKAGE LABEL : EVERYDAY EVERYWHERE HAND SANITIZER GEL 500mL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    EVERYDAY EVERYWHERE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74776-020
    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)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Glycerin (UNII: PDC6A3C0OX)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Polysorbate 80 (UNII: 6OZP39ZG8H)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74776-020-021 in 1 CARTON05/01/2020
    1NDC:74776-020-0160 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:74776-020-03500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/01/2020
    Labeler - C&N COSMETICS CO.,LTD (688853696)
    Registrant - C&N COSMETICS CO.,LTD (688853696)
    Establishment
    NameAddressID/FEIBusiness Operations
    C&N COSMETICS CO.,LTD688853696manufacture(74776-020)
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