Label: CANDICIDE 12X liquid

  • 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 November 7, 2011

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  • ACTIVE INGREDIENT

    Active Ingredients (HPUS): Baptisia Tinctoria 3X, Borax 30X,
    Calcarea Carbonica 30X, Candida Albicans 12X, Kreosotum 30X,
    Lycopodium Clavatum 30X, Nux Vomica 30X, Phosphoricum
    Acidum 30X, Pulsatilla 30X, Sepia 30X. 

  • PURPOSE


    Purpose:     Support for the Treatment of Symptoms Associated with
    Candida Albicans.
  • INDICATIONS & USAGE

    Use: This product is a Homeopathic Dilution, formulated to help
    improve the body’s immunity in the treatment of diagnosed
    Candida Albicans.
  • WARNINGS

    Warnings:

    Use only as directed.


    Stop use and ask a doctor if symptoms worsen or do not
    improve after 5 days.

    Do not use this product, if you have abdominal pain, fever, or foul
    smelling discharge. You may have a condition which is more serious.

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

    Keep out of reach of children. In case of overdose, get medical
    help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION


    Directions:Adults (12 and Older) take 15 drops under the
    tongue three times daily. Children (11 and Younger) take 10 drops
    under the tongue three times daily or as directed by your health
    care professional. Consult a Physician for use in children under
    12 years of age. Not Recommended for Children Under 2
    Years of Age.
  • OTHER SAFETY INFORMATION

    Other Information: Do not use if TAMPER EVIDENT seal
    around neck of bottle is missing or broken.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Demineralized water and 25% USP Ethanol.

  • PRINCIPAL DISPLAY PANEL

     
    Manufactured for PROGENA Professional Formulations
    4820 Eubank Blvd. NE, ABQ., NM 87111, www.progena.com
    image of label

  • INGREDIENTS AND APPEARANCE
    CANDICIDE 12X 
    candicide 12x liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62713-925
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT3 [hp_X]  in 1 mL
    SODIUM BORATE (UNII: 91MBZ8H3QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BORATE30 [hp_X]  in 1 mL
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE30 [hp_X]  in 1 mL
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS12 [hp_X]  in 1 mL
    WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE30 [hp_X]  in 1 mL
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE30 [hp_X]  in 1 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED30 [hp_X]  in 1 mL
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID30 [hp_X]  in 1 mL
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS30 [hp_X]  in 1 mL
    SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62713-925-0130 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/01/1984
    Labeler - Meditrend, Inc. DBA Progena Professional Formulations (130104805)
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