Label: CLAIRFORE- l-ascorbic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 31, 2020

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  • ACTIVE INGREDIENT

    L-ascorbic acid

  • INACTIVE INGREDIENT

    Water, chitosan, egg white hydrolysate

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • PURPOSE

    hand sanitizer to help reduce bacteria that potentially can cause disease

    for use when soap and water are not available

  • INDICATIONS & USAGE

    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.

  • WARNINGS

    For external use only.

    Flammable, keep away from fire or flame.

    When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

    Stop use and ask a doctor if significant irritation or sensitization develops.

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

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLAIRFORE 
    l-ascorbic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75768-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75768-0002-1100 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/01/2020
    Labeler - ORGANELLE Inc (695719718)
    Registrant - ORGANELLE Inc (695719718)
    Establishment
    NameAddressID/FEIBusiness Operations
    ORGANELLE Inc695719718manufacture(75768-0002) , label(75768-0002)