Label: PINE PHYTONCIDE ANTISEPTIC SOLUTION- pinus densiflora extract 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 April 28, 2020

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

  • ACTIVE INGREDIENT

    Pinus Densiflora Extract

  • INACTIVE INGREDIENT

    Water

  • PURPOSE

    antibiosis

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    Store under 30°C (86°F)

  • 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

    Spray well using on objects for sterilization.

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    PINE PHYTONCIDE ANTISEPTIC SOLUTION 
    pinus densiflora extract liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74340-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PINUS DENSIFLORA WHOLE (UNII: U797H98B8Y) (PINUS DENSIFLORA WHOLE - UNII:U797H98B8Y) PINUS DENSIFLORA WHOLE20 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74340-0001-1500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/01/2020
    Labeler - Jungwon Company (694119406)
    Registrant - Jungwon Company (694119406)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jungwon Company694119406manufacture(74340-0001)