Label: COLD- baptisia tintoria root, echinacea angustifolia, eupatoriom perfoliatum flowering top, lomatium dissectum root, pueraria montana var. lobata root, trifolium pratense flower, pnytolacca americana root, onion, arsenic triiodode, barium carbonate, bromide, oyster shell calcium carbonate crude, potassium chloride, mercurius solubilis, silicon dioxide 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 January 28, 2013

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS: Baptisia Tinctoria 3X, Echinacea Angustifolia 3X, Eupatorium Perfoliatum 3X, Lomatium Dissectum 3X, Pueraria Lobata 3X, Trifolium Pratense 3X, Phytolacca Decandra 6X, Allium Cepa 12X, Arsenicum Iodatum 12X, Baryta Carbinica 12 X, Bromium 12X, Calcarea Carbonica 12X, Kali Muriaticum 12X, Lachesis Mutus 12X, Mercuris Solubilis 12X, Silicea 12X

  • PURPOSE

    USES: Temporarily relievews symptoms associated with with the common cold.

  • KEEP OUT OF REACH OF CHILDREN

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

  • INDICATIONS & USAGE

    USES: Temporarily relieves symptoms associated with the common cold.

  • WARNINGS

    WARNING:

    Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING, as a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidential ingestion) get medical help or cantact a Poison control Center right away.

  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Adults and children above 12 years: 10 drops orally 3 times daily, or as directed by a health care prosessional.

  • INACTIVE INGREDIENT

    INACTIVE INGRIDENTS: Purified Warter, USP Ethanol Alcohol 20%

  • PRINCIPAL DISPLAY PANEL

    NDC: 43406-0069-1

    ​COLD

    Copmmon Cold

    HOMEOPATHIC

    1 fl oz (30 mL) / 20% Alcohol

    8 77730 00095 8

    Image of Label

  • INGREDIENTS AND APPEARANCE
    COLD 
    baptisia tintoria root, echinacea angustifolia, eupatoriom perfoliatum flowering top, lomatium dissectum root, pueraria montana var. lobata root, trifolium pratense flower, pnytolacca americana root, onion, arsenic triiodode, barium carbonate, bromide, oyster shell calcium carbonate crude, potassium chloride, mercurius solubilis, silicon dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43406-0069
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT3 [hp_X]  in 1 mL
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA3 [hp_X]  in 1 mL
    EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP3 [hp_X]  in 1 mL
    PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C) (PUERARIA MONTANA VAR. LOBATA ROOT - UNII:PET93F4I3C) PUERARIA MONTANA VAR. LOBATA ROOT3 [hp_X]  in 1 mL
    TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (TRIFOLIUM PRATENSE FLOWER - UNII:4JS0838828) TRIFOLIUM PRATENSE FLOWER3 [hp_X]  in 1 mL
    PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT6 [hp_X]  in 1 mL
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION12 [hp_X]  in 1 mL
    ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC CATION (3+)12 [hp_X]  in 1 mL
    BARIUM CARBONATE (UNII: 6P669D8HQ8) (BARIUM CATION - UNII:V645272HLN) BARIUM CATION12 [hp_X]  in 1 mL
    BROMINE (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G) BROMINE12 [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
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE12 [hp_X]  in 1 mL
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM12 [hp_X]  in 1 mL
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS12 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43406-0069-130 mL in 1 BOTTLE, DROPPER
    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(43406-0069)