Label: INFLAMMATION (arnica montana, benzoicum acidum, echinacea (angustifolia), apis mellifica, baptisia tinctoria, dulcamara, eucalyptus globulus, solanum nigrum, eupatorium perfoliatum, bryonia- alba, colchicum autumnale, mercurialis perennis, rhus tox liquid

  • NDC Code(s): 43742-1303-1
  • 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 March 5, 2024

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  • ACTIVE INGREDIENTS:

    Arnica Montana 3X, Benzoicum Acidum 3X, Echinacea (Angustifolia) 3X, Apis Mellifica 4X, Baptisia Tinctoria 4X, Dulcamara 4X, Eucalyptus Globulus 4X, Solanum Nigrum 4X, Eupatorium Perfoliatum 6X, Bryonia (Alba) 8X, Colchicum Autumnale 8X, Mercurialis Perennis 8X, Rhus Tox 8X.

  • HOMEOPATHIC INDICATIONS:

    For temporary relief of inflamed painful or stiff joints, muscle pain, headache, cough, or fever.**

    **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 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 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 of inflamed painful or stiff joints, muscle pain, headache, cough, or fever.**

    **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 43742-1303-1

    HOMEOPATHIC

    INFLAMMATION

    1 FL OZ (30 ml)

    Inflammation

  • INGREDIENTS AND APPEARANCE
    INFLAMMATION 
    arnica montana, benzoicum acidum, echinacea (angustifolia), apis mellifica, baptisia tinctoria, dulcamara, eucalyptus globulus, solanum nigrum, eupatorium perfoliatum, bryonia (alba), colchicum autumnale, mercurialis perennis, rhus tox liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-1303
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA WHOLE3 [hp_X]  in 1 mL
    BENZOIC ACID (UNII: 8SKN0B0MIM) (BENZOIC ACID - UNII:8SKN0B0MIM) BENZOIC ACID3 [hp_X]  in 1 mL
    ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA WHOLE3 [hp_X]  in 1 mL
    APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA4 [hp_X]  in 1 mL
    BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT4 [hp_X]  in 1 mL
    SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP4 [hp_X]  in 1 mL
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF4 [hp_X]  in 1 mL
    SOLANUM NIGRUM WHOLE (UNII: 0FMD6WV47M) (SOLANUM NIGRUM WHOLE - UNII:0FMD6WV47M) SOLANUM NIGRUM WHOLE4 [hp_X]  in 1 mL
    EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP6 [hp_X]  in 1 mL
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT8 [hp_X]  in 1 mL
    COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6) COLCHICUM AUTUMNALE BULB8 [hp_X]  in 1 mL
    MERCURIALIS PERENNIS WHOLE (UNII: Q35465A1MA) (MERCURIALIS PERENNIS - UNII:Q35465A1MA) MERCURIALIS PERENNIS WHOLE8 [hp_X]  in 1 mL
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF8 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-1303-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/10/201812/01/2028
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/10/201812/01/2028
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-1303) , api manufacture(43742-1303) , label(43742-1303) , pack(43742-1303)
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