Label: SKIN SUPPLY HAND SANITIZER- alcohol liquid

  • 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 25, 2020

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

View All Sections
  • Active Ingredient

    Ethanol 77%

  • Purpose

    Antiseptic

  • Use

    Hand sanitizer to help reduce bacteria on skin

  • Warnings

    For external use on hands.

    Flammable. Keep away from fire.

  • Warnings

    Do not use in or near the eyes. In case of contact, rinse with water.

  • Warnings

    Stop use and ask a doctor if irritation or rash appears and lasts.

  • Warnings

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

  • Directions

    Put product onto palm and then rub hands together.

    Children under 6 years of age should be supervised when using this product.

  • Inactive Ingredients

    Water, Glycerin, Ammonium Acryloyldimethyltaurate/VP Copolymer, Eucalyptus Globulus Leaf Oil, Aloe Barbadensis Leaf Juice, Chlorhexidine Digluconate, Sodium Chloride, Glucose

  • Package Label

    300ml NDC: 76731-202-01 Label

  • INGREDIENTS AND APPEARANCE
    SKIN SUPPLY HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76731-202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL77 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI) 0.6 mL  in 100 mL
    EUCALYPTUS OIL (UNII: 2R04ONI662) 0.5 mL  in 100 mL
    WATER (UNII: 059QF0KO0R) 18.38 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 3 mL  in 100 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.005 mL  in 100 mL
    ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) 0.005 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.5 mL  in 100 mL
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) 0.01 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76731-202-01300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/28/2020
    Labeler - BBHC CO., LTD (689522401)
    Registrant - STC Nara Co., Ltd (689135085)
    Establishment
    NameAddressID/FEIBusiness Operations
    STC Nara Co., Ltd689135085manufacture(76731-202)
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!