Label: HEALING WATERS VIOLET ROSE HAND SANITIZER- alcohol liquid

  • Category: HUMAN PRESCRIPTION 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 February 9, 2010

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

View All Sections
  • DOSAGE & ADMINISTRATION

    Directions:

    Rub a small amount onto palms of hands to kill unwanted germs and bacteria


  • INACTIVE INGREDIENT

    Ingredients:

    Alcohol, Water, Carbomer, Triethanolamine, Fragrance, Tocopheryl Acetate, Cellulose, FD and C Blue No. 1, D and C Red No. 33

  • DESCRIPTION

    Formulated Exclusively and Distributed by:

    Enchante Accessories, Inc., New York, NY 10016

    Not Tested on Animals. For Adult Use Only.

    Designed in the USA. Made in China.



  • PRINCIPAL DISPLAY PANEL

    piclabel

  • INGREDIENTS AND APPEARANCE
    HEALING WATERS VIOLET ROSE HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:22100-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 39.1996 g  in 100 g
    CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC) 0.2 g  in 100 g
    TROLAMINE (UNII: 9O3K93S3TK) 0.2 g  in 100 g
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) 0.1 g  in 100 g
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) 0.1 g  in 100 g
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.0001 g  in 100 g
    ROSE PETAL EXTRACT (UNII: 969IQC5YJU) 0.2 g  in 100 g
    D&C RED NO. 33 (UNII: 9DBA0SBB0L) 0.0003 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22100-006-0129 g in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33302/20/2010
    Labeler - Ningbo Meiduo General Products Co., Ltd (547230008)
    Registrant - Ningbo Meiduo General Products Co., Ltd (547230008)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Meiduo General Products Co., Ltd547230008manufacture
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!