GUM DROP HAND SANITIZER (ETHYL ALCOHOL) LIQUID [PAPERMATES, INC. DBA NOTEWORTHY]

GUM DROP HAND SANITIZER (ETHYL ALCOHOL) LIQUID [PAPERMATES, INC. DBA NOTEWORTHY]
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NDC 75997-027-01
Set ID 21e4d3a5-86f1-4d6f-998c-9055fd50ca94
Category HUMAN OTC DRUG LABEL
Packager Papermates, Inc. dba Noteworthy
Generic Name
Product Class
Product Number
Application Number PART333A
  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Sanitizer

  • Uses

    To decrease bacteria on the skin that could cause disease.

    recommended for repeated use

  • Warnings

    For external use only-hands. Use only as directed. Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash redness or itching occurs

    Flammable. keep away from heat and flame.

  • When using this product

    keep out of eyes. In case of contact with eyes immediately flush with water and call a doctor

    avoid contact with broken skin.

  • STOP USE

    Stop use and ask a doctor if irritation or redness develops.

  • Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • Directions

    put a thumb size amount in your palm and rub hands together briskly until dry. recommended for repeated use.

  • Other Information

    do not store in temperatures over 118F.

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

    may discolor certain fabrics.

  • Inactive Ingredients

    aloe barbadensis gel, blue 1, carbomer, deionized water, fragrance, glycerin, propylene glycol, red 33, triethanolamine and vitamin E

  • PRINCIPAL DISPLAY PANEL

    Gum Drop
    Hand sanitizer

    net .95fl oz (28ml)

  • PRINCIPAL DISPLAY PANEL

    Vanilla Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    GUM DROP HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75997-027
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE (UNII: V5VD430YW9)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75997-027-0128 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/28/2011
    Labeler - Papermates, Inc. dba Noteworthy (038734620)

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