YEAST GARD ADVANCED (BERBERIS VULGARIS, BORAX, COLLINSONIA CANADENSIS, HAMAMELIS VIRGINIANA) DOUCHE [WISCONSIN PHARMACAL COMPANY]

YEAST GARD ADVANCED (BERBERIS VULGARIS, BORAX, COLLINSONIA CANADENSIS, HAMAMELIS VIRGINIANA) DOUCHE [WISCONSIN PHARMACAL COMPANY]
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NDC 68093-0668-1
Set ID 0dfe58cd-713c-4a0d-88e2-1604fe13292a
Category HUMAN OTC DRUG LABEL
Packager Wisconsin Pharmacal Company
Generic Name
Product Class
Product Number
Application Number
  • Active Ingredients

    Borax 3X HPUS
    Collinsonia Canadensis 3X HPUS
    Berberis Vulgaris 6X HPUS
    Hamamelis Virginiana 6X HPUS

  • PURPOSE

    Purpose

    Temporary relief from vaginal itching, burning and irritation

  • Uses

    Uses For the temporary relief of symptoms associated with vagianl yeast infection, including:

    • itching
    • burning
    • irritation
  • Warnings

    • Use only as directed
    • For vaginal use only

    Ask a doctor before use if you have

    • Vaginal itching and discomfort for the first time
    • Lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge. You may have a serious condition.
    • Vaginal yeast infections often (such as once a month or 3 in 6 months). You could be pregnant or have a serious underlying medical cause for you symptoms, including diabetes or a weakened immune system.
    • Been exposed to the human immunodeficiency virus (HIV) that causes AIDS
    • You have an STD (sexually transmitted disease) or PID (Pelvic inflammatory disease)
    • You have frequent and painful urination

    Stop use and ask a doctor if:

    • Symptoms last more than 7 days
    • You get a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vagina.

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children.

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

    Do not use

    • if you have never had a vaginal yeast infection diagnosed by a doctor

    When using this product

    • if you do not get complete relief ask a doctor before using another product
  • Directions

    Directions

    Tamper Evident: If the foil seal on bottle opening is missing, torn or damaged in any way, do not use.

    • Wash hands thoroughly with soap and water before and after use
    • remove cap and safety seal from bottle. Carefully open teh packet and pour homeopathic contents into the douche bottle. Screw cap back onto bottle and shake thoroughly to fully mix powder into solution. After fully mixed, remove cap. Remove sanitary wrap from nozzle. Screw nozzle onto douche bottle.
    • Slowly insert nozzle into vagina about 3 inches. If needed, a small amount of personal lubricant can be applied to nozzle to ease insertion of nozzle into vagina. Gently squeeze bottle until solution is dispensed. Use while sittion on the toilet, standing in the shower or in the tub. After douching discard bottle and nozzle.

  • OTHER SAFETY INFORMATION

    Other information

    • a douche is not a contraceptive and should not be used to prevent pregnancy
    • do not use if foil seal on bottle opening is missing, torn damaged in any way. use if homeopathic packet is torn, open or incompletely sealed. purchase if carton is open
    • Store at room temperature
    • Lot number and expiration date: see upper back panel of box
    • There is no scientific evidence that this product works. Ther product claims are based on theories of homeopathy from the 1700's that are not accepted by most modern medical experts.

  • Inactive ingredients

    Bacillus coagulans, citric acid, edetate disodium, maltodextrin, purified water, sodium benzoate, sodium lauryl sulfate, trisodium phosphate

  • QUESTIONS

    Questions or commetns? 1-800-635-3696

  • PRINCIPAL DISPLAY PANEL

    Carton

  • INGREDIENTS AND APPEARANCE
    YEAST GARD ADVANCED 
    berberis vulgaris, borax, collinsonia canadensis, hamamelis virginiana douche
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68093-0668
    Route of AdministrationVAGINAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK6 [hp_X]  in 1 g
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK6 [hp_X]  in 1 g
    SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22) SODIUM BORATE3 [hp_X]  in 1 g
    COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (COLLINSONIA CANADENSIS ROOT - UNII:O2630F3XDR) COLLINSONIA CANADENSIS ROOT3 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    BACILLUS COAGULANS (UNII: ISK1LOY57E)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68093-0668-12 in 1 CARTON10/01/2007
    1133.07 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/01/2007
    Labeler - Wisconsin Pharmacal Company (800873986)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wisconsin Pharmacal Company800873986manufacture(68093-0668)

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