Label: DIZZINESS HP- oyster shell calcium carbonate crude, chenopodium ambrosioides, anamirta cocculus seed, conium maculatum flowering top, strychnos nux-vomica seed, phosphorus, pulsatilla vulgaris, silicon dioxide liquid

  • NDC Code(s): 43406-0017-1
  • Packager: Natural Creations, 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 January 5, 2023

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Calcarea Carbonica 30X, Cheopodium Anthelminticum 30X, Cocculus Indicus 30X, Conium Maculatum 30X, Nux Vomica 30X, Phosphorus 30X, Pulsatilla 30X, Silicea 30X

  • PURPOSE

    USES: Temporarily relieves dizziness and nausea.**

  • INDICATIONS & USAGE

    USES: Temporarily relieves dizziness and nausea.**

  • DOSAGE & ADMINISTRATION

    Directions:  Adults & children above 12 years:  10 drops orally 3 times daily, or as directed by a health care professional.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN.  In case of overdose (or accidental ingestion) get    medical help or contact a Poison Control Center right away

  • WARNINGS

    WARNINGS:

    •   Consult a physician for use in children under 12 years of age.
    • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
    • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
    • Do not use if TAMPER EVIDENT seal is broken or missing.
  • INACTIVE INGREDIENT

    Inactive Ingredients:  Purified Water, USP Ethanol Alcohol 20%

  • QUESTIONS

    Questions & Comments?  Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

  • REFERENCES

    *The  letters “HPUS” indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • PRINCIPAL DISPLAY PANEL

    NDC: 43406-0017-1

    DIZZINESS HP

    HOMEOPATHIC

    1 fl oz (30 mL) 20% Alcohol

    image of label

  • INGREDIENTS AND APPEARANCE
    DIZZINESS HP 
    oyster shell calcium carbonate crude, chenopodium ambrosioides, anamirta cocculus seed, conium maculatum flowering top, strychnos nux-vomica seed, phosphorus, pulsatilla vulgaris, silicon dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43406-0017
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE30 [hp_X]  in 1 mL
    CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (CHENOPODIUM AMBROSIOIDES - UNII:4H5RSU087I) CHENOPODIUM AMBROSIOIDES30 [hp_X]  in 1 mL
    ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED30 [hp_X]  in 1 mL
    CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371) CONIUM MACULATUM FLOWERING TOP30 [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
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS30 [hp_X]  in 1 mL
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS30 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43406-0017-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/29/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/29/2007
    Labeler - Natural Creations, Inc. (018022074)
    Establishment
    NameAddressID/FEIBusiness Operations
    OHM Pharma, Inc.030572478manufacture(43406-0017)
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