Label: PEMF OPTIMIZER- aqua sulis, argentum metallicum, aurum metallicum, cuprum metallicum, lapis albus, manganum metallicum vanadium metallicum viscum album, zincum metallicum liquid

  • NDC Code(s): 43742-0693-1
  • 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 January 15, 2024

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  • ACTIVE INGREDIENTS:

    Aqua Sulis 30C, 200C, 1M, 10M, Argentum Metallicum 1M, 10M, Aurum Metallicum 1M, 10M, Cuprum Metallicum 1M, 10M, Lapis Albus 1M, 10M, Manganum Metallicum 1M, 10M, Vanadium Metallicum 1M, 10M, Viscum Album 1M, 10M, Zincum Metallicum 1M, 10M.

  • HOMEOPATHIC INDICATIONS:

    For temporary relief from the symptoms associated with exposure to PEMF, including vertigo, light sensitivity, mood swings, and poor memory.**

    **These statements are based upon 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 a physician or 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 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.

  • HOMEOPATHIC INDICATIONS:

    For temporary relief from the symptoms associated with exposure to PEMF, including vertigo, light sensitivity, mood swings, and poor memory.**

    **These statements are based upon 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 43742-0693-1

    HOMEOPATHIC

    PEMF

    OPTIMIZER

    1 FL OZ (30 ml)

    PEMF Optimizer

  • INGREDIENTS AND APPEARANCE
    PEMF OPTIMIZER 
    aqua sulis, argentum metallicum, aurum metallicum, cuprum metallicum, lapis albus, manganum metallicum vanadium metallicum viscum album, zincum metallicum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-0693
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER30 [hp_C]  in 1 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER1 [hp_M]  in 1 mL
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD1 [hp_M]  in 1 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER1 [hp_M]  in 1 mL
    CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3) (CALCIUM HEXAFLUOROSILICATE - UNII:2NVP93XVQ3) CALCIUM HEXAFLUOROSILICATE1 [hp_M]  in 1 mL
    MANGANESE (UNII: 42Z2K6ZL8P) (MANGANESE - UNII:42Z2K6ZL8P) MANGANESE1 [hp_M]  in 1 mL
    VANADIUM (UNII: 00J9J9XKDE) (VANADIUM - UNII:00J9J9XKDE) VANADIUM1 [hp_M]  in 1 mL
    VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP1 [hp_M]  in 1 mL
    ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC1 [hp_M]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-0693-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product12/08/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/08/2015
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-0693) , api manufacture(43742-0693) , label(43742-0693) , pack(43742-0693)
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