Label: WASHJO ROSEMARY FREE HAND DISINFECTANT 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 22, 2020

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  • Active Ingredient(s)

    Ethanol 75%

  • Purpose

    Antiseptic

  • Uses

    Rosemary Wash Free Disinfection Gel to help reduce bacteria that potentially can cause disease.For use when soap and water are

    not available.

  • WARNINGS

    Keep out of reach of children unless supervised by an adult.

  • Do not use

  • WHEN USING

  • STOP USE

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

  • Other information

    1.Store between 15-30C(59-86F) ;

    2.May discolor certain fabrics or surfaces;

    3.Avoid freezing and excessive heat above 40C(104F)

  • INACTIVE INGREDIENTS

    Rosemary essential oil,Eucalyptus essential oil, rosemary extract,ethanol,glycerin, aloe extract.

  • Package Label - Principal Display Panel

    70 ml label 100 ml label250 ml label 300 ml label 350 ml label 500 ml label

  • INGREDIENTS AND APPEARANCE
    WASHJO ROSEMARY FREE HAND DISINFECTANT 
    washjo rosemary free hand disinfectant gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75824-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE (UNII: V5VD430YW9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75824-005-0170 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    2NDC:75824-005-03250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    3NDC:75824-005-02100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    4NDC:75824-005-04300 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    5NDC:75824-005-05350 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    6NDC:75824-005-06500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/22/2020
    Labeler - Shenzhen Flowerset Cosmetics Co., Ltd (417323188)
    Registrant - Shenzhen Flowerset Cosmetics Co., Ltd (417323188)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Flowerset Cosmetics Co., Ltd417323188manufacture(75824-005)
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