Label: RHEUMATISM (benzoicum acidum, rhododendron chrysanthum, spiraea ulmaria, aconitum napellus, dulcamara, ledum palustre, pulsatilla- vulgaris, asclepias tuberosa, lithium benzoicum, euphorbium officinarum liquid

  • NDC Code(s): 43742-1221-1
  • 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 December 5, 2023

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  • ACTIVE INGREDIENTS:

    Benzoicum Acidum 3X, Spiraea Ulmaria 3X, Aconitum Napellus 4X, Dulcamara 4X, Ledum Palustre 4X, Pulsatilla (Vulgaris) 4X, Asclepias Tuberosa 6X, Lithium Benzoicum 8X, Euphorbium Officinarum 9X, Rhododendron Chrysanthum 10X.

  • HOMEOPATHIC INDICATIONS:

    For temporary relief of symptoms related to rheumatism including joint pain, fever, inflammation and pain of leg(s).**

    **These statements are based upon traditional 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 a 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 a 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 symptoms related to rheumatism including joint pain, fever, inflammation and pain of leg(s).**

    **These statements are based upon traditional 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 43742-1221-1
    HOMEOPATHIC
    RHEUMATISM
    1 FL OZ (30 ml)

    image description

  • INGREDIENTS AND APPEARANCE
    RHEUMATISM 
    benzoicum acidum, rhododendron chrysanthum, spiraea ulmaria, aconitum napellus, dulcamara, ledum palustre, pulsatilla (vulgaris), asclepias tuberosa, lithium benzoicum, euphorbium officinarum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43742-1221
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOIC ACID (UNII: 8SKN0B0MIM) (BENZOIC ACID - UNII:8SKN0B0MIM) BENZOIC ACID3 [hp_X]  in 1 mL
    FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (FILIPENDULA ULMARIA ROOT - UNII:997724QNDS) FILIPENDULA ULMARIA ROOT3 [hp_X]  in 1 mL
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS4 [hp_X]  in 1 mL
    SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP4 [hp_X]  in 1 mL
    RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) RHODODENDRON TOMENTOSUM LEAFY TWIG4 [hp_X]  in 1 mL
    ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) ANEMONE PULSATILLA4 [hp_X]  in 1 mL
    ASCLEPIAS TUBEROSA ROOT (UNII: 1ZL82U5D18) (ASCLEPIAS TUBEROSA ROOT - UNII:1ZL82U5D18) ASCLEPIAS TUBEROSA ROOT6 [hp_X]  in 1 mL
    LITHIUM BENZOATE (UNII: R9Z042Z19E) (LITHIUM CATION - UNII:8H8Z5UER66) LITHIUM BENZOATE8 [hp_X]  in 1 mL
    EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (EUPHORBIA RESINIFERA RESIN - UNII:1TI1O9028K) EUPHORBIA RESINIFERA RESIN9 [hp_X]  in 1 mL
    RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U) RHODODENDRON AUREUM LEAF10 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43742-1221-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/29/201811/21/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/29/201811/21/2024
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43742-1221) , api manufacture(43742-1221) , label(43742-1221) , pack(43742-1221)
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