Rheuma DKS

Manufacturer
Uriel Pharmacy Inc.
Effective date
2025-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:31:31

Label at a glance#

ProductRheuma DKS
Active ingredientEQUISETUM ARVENSE TOP, FORMICA RUFA, ONION, ARNICA MONTANA FLOWER, COMFREY ROOT, TIN
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

At first sign of stiffness or painful joints, apply to skin 2-3 times daily or as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100 gm contains: 2.5 gm Allium cepa (Onion) 1X, 2 gm Arnica 1X, 1 gm Symphytum (Comfrey) 1X; Formica (Red wood ant) 4X/8X, Equisetum (Common horsetail) 5X, Stannum met. (Metallic tin) 8X/20X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Lanolin, Beeswax, Sunflower seed oil, Camphor, Birch leaf extract, Chamomile flower extract, Rosemary herb extract, Fir needle oil, Pine needle oil, Rosemary oil, Spring water, Lemon oil, Red copper oxide, Menthol, Peppermint oil, Lavender oil, Tea tree oil, Purified turpentine oil, Grapefruit seed extract, Sage oil, Capsicum oleoresin

Prepared using rhythmical processses.

OTC - PURPOSE SECTION

Use: Temporary relief of stiff and painful joints.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rheuma DKS OintmentRheuma DKS Ointment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8428-5Rheuma DKS60 g in 1 TUBEOINTMENT602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8428RHEUMA DKS OINTMENT [URIEL PHARMACY INC.]2Current NDC, 1 package rows20250124_292a6a25-35a3-cd63-e063-6394a90aa2a3.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-842848951-8428-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
Rheuma DKSRHEUMA DKSUriel Pharmacy Inc.292a6a25-35a3-cd63-e063-6394a90aa2a32025-01-22WarningsExact identifier
ndc (package): 48951-8428-5
ndc (product): 48951-8428
ndc11 (package): 48951842805
spl id: 2c52e64e-d6ec-f256-e063-6294a90a7feb
spl set id: 292a6a25-35a3-cd63-e063-6394a90aa2a3

Reported adverse events (FAERS/openFDA)#

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