Label: PROGESTERONE liquid

  • NDC Code(s): 43742-0851-1
  • Packager: Deseret Biologicals, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 March 14, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENTS:

    Progesterone 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

  • PURPOSE:

    Progesterone - Mood Swings, Painful Menses, Nervousness, Hot Flashes, Headache, Breast Tenderness, Breast Pain, Back Pain, Leg Pain

  • USES:

    • For the temporary relief of symptoms including:

    • mood swings • painful menses • nervousness 

    • hot flashes • headache • breast tenderness

    • breast pain • back pain • let pain

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

  • WARNINGS:

    If pregnant or breast-feeding, seek advice of a health professional before use.

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

    Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

  • KEEP OUT OF REACH OF CHILDREN:

    In case of overdose, contact a physician or Poison Control Center right away.

  • DIRECTIONS:

    1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

  • INACTIVE INGREDIENTS:

    Demineralized water, 25% ethanol

  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.

    469 W. Parkland Drive

    Sandy, UT 84070

    www.desbio.com

    800-827-8204

  • PACKAGE LABEL DISPLAY:

    DesBio

    Progesterone

    Homeopathic

    NDC 43742-0851-1

    1 FL OZ (30 ml)

    Progesterone

  • INGREDIENTS AND APPEARANCE
    PROGESTERONE 
    progesterone liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0851
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y) PROGESTERONE6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-0851-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/19/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/19/2016
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-0851) , api manufacture(43742-0851) , label(43742-0851) , pack(43742-0851)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!