Label: PROGESTERONE PHENOLIC- progesterone liquid

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

Drug Label Information

Updated 03/13

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

  • ACTIVE INGREDIENTS

    Progesterone 6X, 12X, 30X, 12C, 30C

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  • INDICATIONS

    For temporary relief of symptoms of dairy and milk allergies, mood swings, painful menses, breast tenderness, headaches, hot flashes, and nervousness.

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

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  • WARNINGS

    If pregnant or breast-feeding, ask 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.

    Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

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  • DIRECTIONS

    Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

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  • INACTIVE INGREDIENTS

    Demineralized water, 20% Ethanol.

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  • KEEP OUT OF REACH OF CHILDREN

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

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  • INDICATIONS AND USAGE

    For temporary relief of symptoms of dairy and milk allergies, mood swings, painful menses, breast tenderness, headaches, hot flashes, and nervousness.

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

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  • QUESTIONS

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579

    800-869-8078

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  • PRINCIPAL DISPLAY PANEL

    ENERGIQUE

    since 1987

    HOMEOPATHIC REMEDY

    PROGESTERONE PHENOLIC

    1 fl oz. (30 ml)

    Progesterone Phenolic

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  • INGREDIENTS AND APPEARANCE
    PROGESTERONE PHENOLIC 
    progesterone liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0047
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y) PROGESTERONE 6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44911-0047-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 03/11/2013
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(44911-0047)
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