Label: EQUATE YEAST RELIEF- candida albicans, wood creosote, sodium chloride, and sulfur tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 31, 2023

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

  • Active Ingredients

    Candida albicans 30X

    Kreosotum 30X

    Natrium muriaticum 12X

    Sulphur 12X

  • Purpose

    Candida albicans 30X - Relief from vaginal itching, burning and discharge

    Candida albicans 30X - Relief from vaginal itching, burning, odor and discharge

    Kreosotum 30X - Relief from vaginal itching, burning, odor and discharge

    Natrium muriaticum 12X - Relief from vaginal itching, burning, odor and discharge

    Sulphur 12X - Relief from vaginal itching, burning, odor and discharge

  • Uses

    

    See your doctor if this is the first time you have vaginal itching and discomfort to find out if you have a vaginal yeast infection. According to homeopathic indications, these ingredients provide temporary relief of yeast infection related symprtoms such as:

    • itching and burning, occasional vaginal odor and discharge, after consultation by a physician.

    *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

  • Warnings

    For oral use only. This product will not cure a yeast infection. Do not use if you have never had a vaginal yeast infection diagnosed by a doctor. 

  • Stop use and contact your physician if

    • your symptoms do not improve within 3 days or if symptoms last more than 7 days.
    • you get a rash, hives, abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge.
  • Ask Doctor

    A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CONDITIONS.

    • This product is intended to complement, not replace, standard medical treatment.
    • Initial worsening of symptoms may occur.
  • Pregnancy warning

    If pregnant or breastfeeding, ask a health professional before use.

  • Keep out of reach of children

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

  • Directions 

    Adults: take one tablet orally three times a day as long as symptoms persist. Children: consult a doctor prior to use.

    • Take at least 10 minutes before or at least 10 minutes after eating or drinking.
    • For occasional support take one tablet per day.
    • Homeopathic remedies may not be effective for everyone. Individual results may vary.
  • Other Information

    

    • Do not use if blister seal is broken.
    • Store at 15° to 30°C (59° to 86° F).
    • Active ingredients are micro-diluted in accordance with the Hemeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects or contraindications. Tamper evident: tablets sealed in blisters. Do not use if blister is open or damaged.
  • Inactive Ingredients

    Magnesium stearate, and Microcrystalline Cellulose, Sucrose.

  • Questions or comments

    Quesitons? 1-888-287-1915

  • Principal Display Panel

    Carton

  • INGREDIENTS AND APPEARANCE
    EQUATE YEAST RELIEF 
    candida albicans, wood creosote, sodium chloride, and sulfur tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-094
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS30 [hp_X]
    WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE30 [hp_X]
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE12 [hp_X]
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR12 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    SUCROSE (UNII: C151H8M554)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeROUNDSize10mm
    FlavorImprint Code H
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-094-1460 in 1 BOX03/04/2022
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/04/2022
    Labeler - WAL-MART STORES INC (051957769)