Label: SEA AND SKI ADVANCE HAND SANITIZER- ethyl alcohol gel

  • 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 February 19, 2021

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

  • Active Ingredient

    Active Ingredient

    Ethyl alcohol 62%

  • Purpose

    Purpose

    Antispetic

  • Uses

    Uses

    To decrease bacteria on the skin that could cause disease

    Recommended for repeated use

  • Warnings

    Warnings

    For external use only: Hands

    Flammable, keep away from fire or flame

    When using

    When usingWhen using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest

    Stop use

    Stop useStop Use and ask a doctor if irritation or redness develops condition persists for more than 72 hours.

    Keep out of reach of children

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

  • Directions

    Directionswet hands thoroughly with product and allow to dry without wiping for children under 6, use ony under adult supervision not recommeded for infants

  • Other information

    Other informationdo not store above 105­°F may discolor some fabrics harmful to wood finishes and plastics

  • Inactive ingredients

    Inactive ingredientsacrylates copolymer*, aloe barbadensis leaf extract, carbomer*, tocopheryl acetate (vitamin E), triethanolamine, water

    *contains one or more of these ingredients

  • Package Label- Principle Display Panel

    Package Label- Principle Display Panel

  • INGREDIENTS AND APPEARANCE
    SEA AND SKI ADVANCE HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73440-3130
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL2343.46 g  in 3779.78 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (OPAQUE) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73440-3130-13779.78 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/27/2020
    2NDC:73440-3130-23779.78 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/27/2020
    Labeler - Cross-Brands Contract Filling (117871824)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cross Brands Contract Filling117871824label(73440-3130) , manufacture(73440-3130) , pack(73440-3130)