FDA.reportPublic FDA data

Rheumatism

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2018-11-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:47:34

Label at a glance#

ProductRheumatism
Active ingredientBENZOIC ACID, PULSATILLA VULGARIS, RHODODENDRON AUREUM LEAF, FILIPENDULA ULMARIA ROOT, ACONITUM NAPELLUS, SOLANUM DULCAMARA TOP, EUPHORBIA RESINIFERA RESIN, LEDUM PALUSTRE TWIG, ASCLEPIAS TUBEROSA ROOT, LITHIUM BENZOATE
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

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

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

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:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INDICATIONS & USAGE SECTION

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:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070    www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0730-1

HOMEOPATHIC

RHEUMATISM

1 FL OZ (30 ml)

RheumatismRheumatism

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-073043742-0730-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOIC ACID8SKN0B0MIMACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
RHODODENDRON AUREUM LEAFIV92NQJ73UACTIB
FILIPENDULA ULMARIA ROOT997724QNDSACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
SOLANUM DULCAMARA TOPKPS1B1162NACTIB
EUPHORBIA RESINIFERA RESIN1TI1O9028KACTIB
LEDUM PALUSTRE TWIG877L01IZ0PACTIB
ASCLEPIAS TUBEROSA ROOT1ZL82U5D18ACTIB
LITHIUM BENZOATER9Z042Z19EACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b09ef189-41b0-4d09-ba29-b57ad0ca864b6213ffc6-5ca4-4f72-9d1a-d212bec655ae2018-11-07WarningsExact identifier
spl id: b09ef189-41b0-4d09-ba29-b57ad0ca864b
spl set id: 6213ffc6-5ca4-4f72-9d1a-d212bec655ae

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.