Label: DIIZ HAND SANITIZER- alcohol gel

  • 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 May 1, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Active ingredients: Alcohol 70.0%

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Aloe Barbadensis Leaf Extract, Citrus Paradisi (Grapefruit) Seed Extract, Disodium EDTA, Glycerin, Propylene Glycol, Carbomer, 1,2-Hexandiol, Water, Triethanolamine

  • PURPOSE

    PURPOSE: Antimicrobial

  • WARNINGS

    Warnings:

    For external use only

    Flammable. Keep away from heat and flame.

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if skin irritation or rash develops.

  • 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

    ■ Hand sanitizer to reduce bacteria on the skin.

  • Directions

    Directions

    ■ Put enough product in your palm to cover hands and rub hands together briskly until dry.
    ■ Children under 6 years of age should be supervised when using product.

  • Other Information

    Other Information

    ■ Store below 43°C (110°F)
    ■ May discolor certain fabrics or surfaces

  • QUESTIONS

    Questions

    www.sacos.co.kr

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    DIIZ HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74923-080
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol350 mL  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Water (UNII: 059QF0KO0R)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Glycerin (UNII: PDC6A3C0OX)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74923-080-01500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/01/2020
    Labeler - THE SUN CO.LTD (694433104)
    Registrant - THE SUN CO.LTD (694433104)
    Establishment
    NameAddressID/FEIBusiness Operations
    THE SUN CO.LTD694433104manufacture(74923-080)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!