Label: TEETHING COMPLEX- belladonna, calcarea carbonica, calcarea fluorica, chamomilla, ferrum phosphoricum, kreosotum, podophyllum peltatum liquid

  • 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 June 1, 2011

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  • Purpose:

    Suggested use for one or more of the following symptoms:

    Earache pain from teething, low-grade fever, indigestion, cranky moods, also helps cutting teeth.

  • Usage and Dosage:

    For oral use only.

  • DOSAGE & ADMINISTRATION

    Adults:

        In Acute Phase:
                12-15 drops, every half hour until relief occurs
        When Relief Occurs:
                12-15 drops, 4-6 times per day

    Children 2-12 years:

                8-10 drops, 4-6 times per day

    Infants 0-24 months:


                4 drops, 4-6 times per day

  • Warnings:

    Keep out of reach of children.

  • WARNINGS

    If symptoms persist, consult a physician.

    Do not use if ring on bottom of cap is broken or missing.

  • Active Ingredients:

    Belladonna 12X, Calcarea carbonica 12X, Calcarea fluorica 12X, Chamomilla 4X, Ferrum phosphoricum 12X, Kreosotum 6X, Podophyllum peltatum 6X

  • Inactive Ingredients:

    Alcohol, 20% USP

  • QUESTIONS

    Manufactured by Nova Homeopathic Therapeutics Inc., Albuquerque, New Mexico USA 87109
    1-800-225-8094

  • PRINCIPAL DISPLAY PANEL

    Teething Complex Product


    Teething Complex Product

    Teething Complex Bottle Label


    Teething Complex Bottle

    Teething Complex Box


    Teething Complex Box


  • INGREDIENTS AND APPEARANCE
    TEETHING COMPLEX 
    belladonna, calcarea carbonica, calcarea fluorica, chamomilla, ferrum phosphoricum, kreosotum, podophyllum peltatum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52731-7009
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA12 [hp_X]  in 1 mL
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]  in 1 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (CALCIUM FLUORIDE - UNII:O3B55K4YKI) CALCIUM FLUORIDE12 [hp_X]  in 1 mL
    MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA4 [hp_X]  in 1 mL
    FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (FERRUM PHOSPHORICUM - UNII:91GQH8I5F7) FERRUM PHOSPHORICUM12 [hp_X]  in 1 mL
    WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE6 [hp_X]  in 1 mL
    PODOPHYLLUM (UNII: 2S713A4VP3) (PODOPHYLLUM - UNII:2S713A4VP3) PODOPHYLLUM6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52731-7009-21 in 1 BOX
    1NDC:52731-7009-150 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/01/2011
    Labeler - Nova Homeopathic Therapeutics, Inc. (194394540)
    Registrant - Nova Homeopathic Therapeutics, Inc. (194394540)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nova Homeopathic Therapeutics, Inc.194394540manufacture, label, pack
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