Label: CENTECASSOL S.O.S 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 April 10, 2020

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

View All Sections
  • Active ingredient

    Alcohol (60%)

  • Purpose

    Antibacterial

  • Uses

    Uses Hand sanitizer for decreasing bacteria on skin

  • Warnings

    For external use only

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

    When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin. Do not puncture or incinerate.

    Stop use and ask a doctor ifirritation or redness develops and condition persists for more than 72 hours

    If pregnant or breast-feeding, ask a health professional before use.

  • Directions

    Take appropriate amount onto your hand and spread it all the way to fingertips. Rub the contents until it dries

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Inactive ingredients

    Water, Centella Asiatica Extract, Carbomer, Triethanolamine, Melaleuca Alternifolia (Tea Tree) Leaf Oil

  • CENTECASSOL S.O.S SANITIZER (500ml)

    centecassol 500ml

  • INGREDIENTS AND APPEARANCE
    CENTECASSOL S.O.S SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73800-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73800-102-021 in 1 BOX04/10/2020
    1NDC:73800-102-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/10/2020
    Labeler - HANSOLBIO CO., LTD (694046931)
    Registrant - HANSOLBIO CO., LTD (694046931)
    Establishment
    NameAddressID/FEIBusiness Operations
    HANSOLBIO CO., LTD694046931manufacture(73800-102)
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!