Arthritis/Joints

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2023-12-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:19:09

Label at a glance#

ProductArthritis/Joints
Active ingredientPSEUDOGNAPHALIUM OBTUSIFOLIUM, BERBERIS VULGARIS ROOT BARK, BLACK COHOSH, CINCHONA OFFICINALIS BARK, CITRULLUS COLOCYNTHIS FRUIT PULP, LEDUM PALUSTRE TWIG, RANUNCULUS BULBOSUS, HORSE CHESTNUT, SODIUM BORATE, CUPRIC ACETATE, POTASSIUM CARBONATE, PULSATILLA VULGARIS, CLAVICEPS PURPUREA SCLEROTIUM, AMMONIUM CHLORIDE, SILICON DIOXIDE, SILVER, TRIBASIC CALCIUM PHOSPHATE, SUS SCROFA ADRENAL GLAND, MERCURIC OXIDE, SEPIA OFFICINALIS JUICE, ZINC, PALLADIUM, PICRIC ACID, SULFUR, SUS SCROFA CARTILAGE, SUS SCROFA INTERVERTEBRAL DISC, SUS SCROFA BONE MARROW
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

Gnaphalium Polycephalum 3, Berberis Vulgaris 4X, Cimicifuga Racemosa 4X, Cinchona Officinalis 4X, Colocynthis 4X, Ledum Palustre 4X, Ranunculus Bulbosus 4X, Aesculus Hippocastanum 6X, Borax 6X, Cuprum Aceticum 6X, Kali Carbonicum 6X, Pulsatilla (Vulgaris) 6X, Secale Cornutum 6X, Ammonium Muriaticum 8X, Silicea 8X, Argentum Metallicum 10X, Calcarea Phosphorica 10X, Glandula Suprarenalis Suis 10X, Mercurius Praecipitatus Ruber 10X, Sepia 10X, Zinc Metallicum 10X, Palladium Metallicum 12X, Picricum Acidum 12X, Sulphur 30X, Cartilago Suis 12C, Discus Intervertebralis Suis 12C, Medulla Ossis Suis 12C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to arthritis, including rash, itching, tingling, stress headache, fatigue, swelling and joint pain.**

**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 arthritis, including rash, itching, tingling, stress headache, fatigue, swelling and joint pain.**

**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 43742-0946-1

HOMEOPATHIC

ARTHRITIS/

JOINTS

1 FL OZ (30 ml)

Arthritis JointsArthritis Joints

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-094643742-0946-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

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
7a0d3c8d-b1fc-44d0-8adc-3c1486a4758f9aa74974-404a-41e6-80bd-82e5ffb86c992023-12-05WarningsExact identifier
spl id: 7a0d3c8d-b1fc-44d0-8adc-3c1486a4758f
spl set id: 9aa74974-404a-41e6-80bd-82e5ffb86c99

Reported adverse events (FAERS/openFDA)#

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