Label: DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER ALCOHOL ANTISEPTIC- alcohol liquid

  • NDC Code(s): 23667-102-00
  • Packager: Formulated Solutions, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 29, 2023

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

View All Sections
  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 77% v/v

    Purpose

    Antiseptic

  • Uses(s)

    Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Extermely flammable, do not use near heat or flame or while smoking.

    Do not use

    • On children less than 2 months of age
    • On open skin wounds

    When using this product

    • keep out of eyes, ears, and mouth
    • In case of contact with eyes, rinse eyes thoroughly with water.
    • Do not puncture or incinerate
    • Contents under pressure
    • Do not expose to heat or store at temperatures above 120°F (49°C)

    Stop use and ask a doctor

    • If irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30°C (59-86°F)
    • Avoid freezing and excessive heat beyond 40°C (104°F)
  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, HYdroxyethyl Urea, Tocopheryl Acetate, Water

  • Package Labeling:

    Bottle3

  • INGREDIENTS AND APPEARANCE
    DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER ALCOHOL ANTISEPTIC 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:23667-102
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:23667-102-00166 mL in 1 BOTTLE; Type 0: Not a Combination Product02/09/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/09/2021
    Labeler - Formulated Solutions, LLC (143266687)
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!