Label: ENMOTION FOAM HAND SANITIZER W-MOISTURIZERS, FRAGRANCE FREE- alcohol soap

  • 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 January 25, 2018

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Uses

    • To decrease bacteria on skin that could cause disease
    • Recommended for repeated use
  • Warnings

    • FLAMMABLE, keep away from fire or flame
    • For external use only

    When using this product do not use in or near eyes.

    Stop use if irritation or redness develops. If condition persists for more than 72 hours consult a doctor.

    Keep out of reach of children.
    If swallowed, seek immediate medical attention or call a poison control center.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Inactive Ingredients

    Water(Aqua), DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, FD&C Blue No.1, FD&C Yellow No.5.

  • SPL UNCLASSIFIED SECTION

    Warning: This product contains a chemical known to the state of California to cause cancer.

  • PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label enMotion® Foam Hand Sanitizer with Moisturizers Fragrance Free, Light Green 2-1000 mL(33.8 FL OZ)

    image description
  • INGREDIENTS AND APPEARANCE
    ENMOTION FOAM HAND SANITIZER W-MOISTURIZERS, FRAGRANCE FREE 
    alcohol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-699
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-699-381000 mL in 1 BAG; Type 0: Not a Combination Product01/01/2000
    2NDC:54622-699-1245 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2000
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2000
    Labeler - Georgia-Pacific Consumer Products LP (806142217)
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!