Label: NANOMIX NANO CLEAN- witch hazel soap

  • Category: HUMAN OTC DRUG LABEL

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 December 26, 2012

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredients: Witch hazel (0.001%)

  • INACTIVE INGREDIENT

    Inactive Ingredients:
    Coconut chip, Grape’s seed Oil, Tea Tree Leaf’s Oil, Jojoba Oil, Eriocephalus Punctulatus Oil, Phytosqualane, Tocopherol, Aloe Barbadensis Leaf Extract, Mentha Arvensis Extract, Ginkgo biloba Leaf Extract, Perfume, Organic Germanium, Organic Selenium, Silver, Oriental Herb Extract

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings: Don't use if redness or irritation occur.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children:
    Keep out of reach of babies and children.

  • INDICATIONS AND USAGE

    Indication and usage:
    Do not place a lot of water or moisture before and after use.

  • DOSAGE AND ADMINISTRATION

    Dosage and administration:
    Made enough foam with hands and rubbed on the face or body, and washing with water.

  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    NANOMIX NANO CLEAN 
    witch hazel soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54170-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Witch hazel (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL0.001 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    COCONUT (UNII: 3RT3536DHY)  
    GRAPE SEED OIL (UNII: 930MLC8XGG)  
    JOJOBA OIL (UNII: 724GKU717M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54170-100-01100 g in 1 CARTON
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34709/01/2012
    Labeler - NANOPOLY CO., LTD. (687162537)
    Registrant - NANOPOLY CO., LTD. (687162537)
    Establishment
    NameAddressID/FEIBusiness Operations
    NANOPOLY CO., LTD.687162537manufacture(54170-100)
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

More Info on this Drug

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