Label: LEVOTHYROXINE liquid

  • NDC Code(s): 43742-0955-1
  • Packager: Deseret Biologicals, Inc.
  • 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 13, 2023

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  • ACTIVE INGREDIENT:

    Levothyroxine 16X

  • HOMEOPATHIC INDICATIONS:

    For the temporary relief of symptoms such as backache, constipation, and vomiting.**

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

  • WARNINGS:

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

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

    Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, contact physician or a 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.

  • HOMEOPATHIC INDICATIONS:

    For the temporary relief of symptoms such as backache, constipation, and vomiting.**

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

  • INACTIVE INGREDIENTS:

    Demineralized Water, 25% Ethanol

  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.
    469 W. Parkland Drive
    Sandy, UT 84070      www.desbio.com

  • PACKAGE LABEL DISPLAY:

    DESBIO

    NDC 43742-0955-1

    HOMEOPATHIC

    LEBOTHYROXINE 16X

    1 FL OZ (30 ml)

    Levothyroxine 16X

  • INGREDIENTS AND APPEARANCE
    LEVOTHYROXINE 
    levothyroxine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0955
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEVOTHYROXINE (UNII: Q51BO43MG4) (LEVOTHYROXINE - UNII:Q51BO43MG4) LEVOTHYROXINE16 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-0955-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/06/201701/18/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/06/201701/18/2026
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-0955) , api manufacture(43742-0955) , label(43742-0955) , pack(43742-0955)
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