Label: ROUND AROUND CYPRESS CLEAN SP RAY CYPRESS FOREST- alcohol liquid

  • NDC Code(s): 81540-070-01, 81540-070-02
  • Packager: CJ Olive Young Corporation
  • 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 August 10, 2022

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

View All Sections
  • ACTIVE INGREDIENT

    Alcohol 20%

  • INACTIVE INGREDIENTS

    C12-14 PARETH-7, TANNIC ACID, WATER, GLYCYRRHIZA GLABRA ROOT EXTRACT, ZINGIBER OFFICINALE ROOT EXTRACT, SCHISANDRA CHINENSIS FRUIT EXTRACT, COPTIS JAPONICA ROOT EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, PROPOLIS WAX, ASIATICOSIDE, CHAMAECYPARIS OBTUSA WATER, FRAGRANCE OIL

  • PURPOSE

    Antiseptic

  • WARNINGS

    ■ For external use only
    ■ If you experience any symptoms such as redness, swelling or itchiness during usage or from exposure to direct sunlight after usage, suspend use and consult a physician
    ■ Do not use on wounds or other areas of skin irritation
    ■ Keep out of reach of children
    ■ Store away from direct sunlight

  • KEEP OUT OF REACH OF CHILDREN

    ■ Keep out of reach of children.

  • Uses

    ■ Helps sterilize and deodorize area for pleasant atmosphere.

  • Directions

    Spray on areas that need sterilization or deodorization. For hard-to-reach areas, spray on dry cloth and rub.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    ROUND AROUND CYPRESS CLEAN SP RAY CYPRESS FOREST 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81540-070
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol20 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    C12-14 PARETH-7 (UNII: R66I1M1LNH)  
    TANNIC ACID (UNII: 28F9E0DJY6)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81540-070-01160 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2022
    2NDC:81540-070-02300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2022
    Labeler - CJ Olive Young Corporation (695640147)
    Registrant - CJ Olive Young Corporation (695640147)
    Establishment
    NameAddressID/FEIBusiness Operations
    AD INTERNATIONAL CORP.688233950manufacture(81540-070)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!