Label: NORTH WOODS DERMA GEL CLEAR- alcohol gel

  • NDC Code(s): 53125-801-04, 53125-801-09, 53125-801-57, 53125-801-88
  • Packager: Superior Chemical Corporation
  • 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 August 20, 2020

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

  • Active Ingredient

    Active Ingredient

    Ethyl Alcohol 70%

  • Uses

    Uses

    • Hand sanitizer to reduce microorganisms on the skin.

    • Use this product when soap and water are not available.

  • Purpose

    Purpose

    Antiseptic

  • Warnings

    Warnings

    • For external use only.

    • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    • FLAMMABLE. This product contains ethyl alcohol. Keep away from

    sources of ignition.

    • Discontinue use if irritation or redness develops.

    • If irritation persists for more than 72 hours, consult a physician.

    • KEEP OUT OF REACH OF CHILDREN.

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

  • Directions

    Directions

    • Read the entire label before using this product.

    • Place enough product on your palm to thoroughly cover your hands.

    • Rub hands together briskly until dry.

  • Inactive Ingredients

    Inactive Ingredients

    Water, PEG/PPG-8/3 Laurate, Gycerin, Carbomer, Tetrahydroxypropylethylendiamine, Fragrance.

  • Warnings

    KEEP OUT OF REACH OF CHILDREN.

  • North Woods Derma Gel Clear

    79604

  • INGREDIENTS AND APPEARANCE
    NORTH WOODS DERMA GEL CLEAR 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53125-801
    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
    PROPYLENE OXIDE (UNII: Y4Y7NYD4BK)  
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)  
    HEXYL SALICYLATE (UNII: 8F78EY72YL)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LIME OIL (UNII: UZH29XGA8G)  
    LEMON OIL (UNII: I9GRO824LL)  
    GRAPEFRUIT OIL (UNII: YR377U58W9)  
    MYRCENE (UNII: 3M39CZS25B)  
    CYCLOHEXANE (UNII: 48K5MKG32S)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    ETHYL ACETATE (UNII: 76845O8NMZ)  
    OCTOXYNOL-9 (UNII: 7JPC6Y25QS)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETOL (UNII: Q4R969U9FR)  
    GERANIOL (UNII: L837108USY)  
    BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    DIHYDROMYRCENOL (UNII: 46L1B02ND9)  
    HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53125-801-57550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/2019
    2NDC:53125-801-043780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/2019
    3NDC:53125-801-09500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/201908/20/2020
    4NDC:53125-801-88500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/01/2019
    Labeler - Superior Chemical Corporation (023335086)
    Registrant - Betco Corporation, Ltd (024492831)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation, Ltd024492831manufacture(53125-801) , label(53125-801)