Label: FOREST SUP- alcohol spray

  • 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 June 25, 2020

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  • Active ingredient

    Ethyl alcohol 65%

  • Purpose

    Antimicrobial

  • Use

    • To decrease bacteria on skin
  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts

    Keep out of reach of children.

  • Other information

    • Store below 110°F (43°C)
    • May discolor certain fabrics or surfaces
  • Directions

    Wet hands thoroughly with product and allow to dry without wiping

  • Inactive ingredients

    Water, Glycerin, Cypress Water, Cypress Essence Oil

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    FOREST SUP 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78799-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.65 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)  
    CUPRESSUS SEMPERVIRENS LEAF OIL (UNII: M7QUY89S4O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78799-001-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/25/2020
    2NDC:78799-001-02300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/25/2020
    3NDC:78799-001-03500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/25/2020
    4NDC:78799-001-041000 mL in 1 CONTAINER; Type 0: Not a Combination Product06/25/2020
    5NDC:78799-001-055000 mL in 1 CONTAINER; Type 0: Not a Combination Product06/25/2020
    6NDC:78799-001-0620000 mL in 1 CONTAINER; Type 0: Not a Combination Product06/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/25/2020
    Labeler - our tree co.ltd (694617517)
    Registrant - our tree co.ltd (694617517)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOOD NATURE CO.,LTD695066948manufacture(78799-001)
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