Label: CLORPACTIN WCS-90- chlorine powder, for solution

  • 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 23, 2022

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  • Active ingredient

    Active Chlorine Derived from Calcium Hypochlorite 3-4%
    Available Chlorine 6-8%

  • Purpose

    Topical Antisepsis

  • Keep Out of Reach of Children

  • Uses

    Topical Antisepsis

  • Warnings

    Caution

    Never use Clorpactin WCS-90 powder as is. This product is intended to be used only as a solution (in water). The powder can cause damage to human tissue, and particularly to infected areas or mucous membrane tissue.

  • Directions

    Add the Clorpactin WCS-90 powder to sterile or deionized water at room temperature (20-25° C.). The powder dissolves slowly in water. As a result even after 2-3 minutes of stirring or mixing some residue of incompletely dissolved product will remain. This residue consists of inactive ingredients and therefore there is no necessity to continue to stir or mix for a longer period of time. This residue can be removed by either filtering the solution through a coarse laboratory filter or allowing the solution to settle for about 5 minutes and then decanting the clear solution for use.

    Storage

    Clorpactin WCS-90 solutions should preferably be used as soon as possible after preparation. If the solution must be stored, it can be kept refrigerated (2-8° C.) for up to 10 days in a capped or sealed plastic or glass container using a non-metallic cap. It can be stored at room temperature (20-25° C.) for up to 3 days after preparation.

    Handling

    As with any chlorinated product, Clorpactin WCS-90 solution should be prepared in a ventilated area and inhalation of the vapors should be minimized. The solution can cause bleaching of fabrics or other materials if splashing or spilling occurs.

  • Inactive ingredients

    sodium acid pyrophosphate, sodium hexametaphosphate, sodium dodecylbenzene sulfonate

    PW018 – Revised August 25, 2021

  • Package/Label Principal Display Panel

    NDC - 0327 -0001 - 10

    THE ULTIMATE TOPICAL BIOTICIDE

    Clorpactin® wcs-90

    BRAND OF OXYCHLOROSENE, SODIUM* • REFRIGERATE UPON ARRIVIAL

    BACTERICIDE • VIRUCIDE
    FUNGICIDE • SPORICIDE
    Contents: 5 - 2 gram bottles

    ACTIVE INGREDIENT:
    ACTIVE CHLORINE DERIVED FROM
    CALCIUM HYPOCHLORITE 3-4%
    AVAILABLE CHLORINE 6-8%

    GUARDIAN LABORATORIES div. of UNITED-GUARDIAN, INC. HAUPPAUGE, NY 11788
    CAUTION: KEEP OUT OF REACH OF CHILDREN
     

    Clorpactin® wcs-90     FOR TOPICAL ANTISEPSIS

    DIRECTIONS: Pour the contents of one bottle into a quart of cool or lukewarm water, in a
    glass or plastic container. Stir or shake for several minutes.
    Use the freshly prepared solution for irrigating the infected area as a rinse, soak or spray.
    Repeat applications with a fresh portion of the solution, or allow to soak for 20 to 30 minutes until symptoms disappear or are relieved.

    SEE ENCLOSED INSERT FOR FURTHER INFORMATION

    Made in U.S.A.

    image-01

    Box Label

  • INGREDIENTS AND APPEARANCE
    CLORPACTIN WCS-90 
    chlorine powder, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0327-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORINE (UNII: 4R7X1O2820) (CHLORINE - UNII:4R7X1O2820) CHLORINE0.16 g  in 2 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0327-0001-105 in 1 BOX01/01/1955
    12 g in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other01/01/1955
    Labeler - United-Guardian, Inc. (050594555)
    Establishment
    NameAddressID/FEIBusiness Operations
    United-Guardian, Inc.050594555MANUFACTURE(0327-0001)