Label: BREEZE 70% ALCOHOL ANTIBACTERIAL WIPES- ethyl 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 September 2, 2020

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

  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Use Decreases bacteria on skin

  • Warnings

    For external use only

    Do not use if you are allergic to any of the ingredients

    Keep pack tightly closed when not in use

    Store in a cool and dry place

    When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Adults and children 2 years and over

    • Apply to hands

    • Allow to dry without wiping

    • Do not flush

    • Use the open product in 3 months

  • Inactive Ingredients

    Waters, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl acetate, Fragrance.

  • SPL UNCLASSIFIED SECTION

    Extra Soft

    WITH ALCOHOL

    ALOE VERA & VIT E

    KILLS MORE THAN 99.9% OF GERMS WITHOUT WATER

    UNAC GROUP KOZMETİK SAN. TİC. LTD. ŞTİ

    Trump Towers Residence No: 12/238 D.No:606

    Şişli, Istanbul- TURKEY - Tel: +90 212 526 68 69

    www.unac.com.tr

    USA DISTRIBUTOR: UNAC INTERNATIONAL INC.

    info@unacusa.com

    MADE IN TURKEY

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    BREEZE  70% ALCOHOL ANTIBACTERIAL WIPES
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74955-028
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74955-028-0170 in 1 CANISTER08/01/2020
    13 g in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/01/2020
    Labeler - COSMOLIVE KOZMETIK SANAYI VE TICARET ANONIM SIRKETI (595671824)
    Establishment
    NameAddressID/FEIBusiness Operations
    COSMOLIVE KOZMETIK SANAYI VE TICARET ANONIM SIRKETI595671824manufacture(74955-028)