Label: BREEZE 70% ALCOHOL ANTIBACTERIAL WIPES- ethyl alcohol cloth

  • NDC Code(s): 74955-027-01
  • Packager: COSMOLIVE KOZMETIK SANAYI VE TICARET ANONIM SIRKETI
  • 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 3, 2020

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

View All Sections
  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Use • Decreases bacteria on skin

  • Warnings

    For external use only

    Keep out of eyes. In case of eye contact, rinse with water.

    If irritation develops, discontinue use. Consult a doctor if irritation persists more than 72 hours.

    If swallowed, seek medical attention or contact a Poison Control Center.

    Avoid direct sunlight.

    Keep out of the reach of children, except with adult supervision.

  • Directions for use

    Thoroughly wipe hands and face as desired.

    Allow to dry without wiping.

    Discard wipe in trash receptacle after use. Do not flush.

  • Other Information

    Keep the pack tightly closed when not in use.

    Store in a cool and dry place.

    Use the opened product within 3 months.

  • Inactive Ingredients

    CAS 64-17-5 Aqua, Glycerin, Aloe Barbadensis Leaf Juice, Parfum.

  • SPL UNCLASSIFIED SECTION

    KILLS 99,9% OF GERMS & BACTERIA

    Containing 70%

    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:74955-027
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74955-027-0156 in 1 PACKET08/01/2020
    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(74955-027)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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