Label: ETHANOL- derma foam excel hand sanitizer soap

  • NDC Code(s): 53125-803-88
  • Packager: Superior Chemical Co DBA NorthWoods
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2024

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  • Active ingredient

    Ethyl Alcohol 70% V/V

  • Warning statement

    Fore external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from heat or flame

  • purpose

    Antiseptic

  • when using directions

    when using this product avoid contact with eyes. if contact occurs, rinsth thoroughly wiht water.

    Stop use and ask a doctor if irriataion or rash occurs

  • inactive ingredients

    Aloe Barbadensis Leaf Juide, D&C Green #5, Fragrance, PER-10 Acrylate/perfluorohexylethly Acrylate copolymer, Perfluoroheexylethyl alcohol, propylene glycol, water

  • keep out of reach of children wording

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

  • Directions for usage and dosage

    Read entire label before using this product

    Place enough product on your palm to thoroughly cover your hands. Rub hands together briskly until dry

  • indications and usage

    Hand sanitizer to reduce microorganisms on the skin.

    Use this product when soap and water are not available

  • principle label

    product label

  • INGREDIENTS AND APPEARANCE
    ETHANOL 
    derma foam excel hand sanitizer soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53125-803
    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
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    2-SEC-BUTYL CYCLOHEXANONE (UNII: 5WA6R1KL5J)  
    WATER (UNII: 059QF0KO0R)  
    4-CYCLOHEXYL-2-METHYL-2-BUTANOL (UNII: HFL24LW6V5)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    HEXYL ACETATE (UNII: 7U7KU3MWT0)  
    TETRAHYDROLINALOOL (UNII: UM4XS5M134)  
    ISOPROPYLPHENYLBUTANAL (UNII: Z92022479Y)  
    2-(PERFLUOROHEXYL)ETHANETHIOL (UNII: 66E2ZQ1P07)  
    PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53125-803-88500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/14/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/14/2024
    Labeler - Superior Chemical Co DBA NorthWoods (023335086)
    Registrant - Betco Corp LLC (005050158)
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