Hendel Rhus Tox

Manufacturer: MediNatura Inc
Effective date: 2022-08-22
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:18:03

Label at a glance#

ProductHendel Rhus Tox

Active ingredientTOXICODENDRON PUBESCENS LEAF

Label structure8 sections

Indications and uses

For the temporary relief of: • Painful Joints • Muscle Aches • Stiffness in Joints

Dosage and administration

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician

Label contents#

Full prescribing information#

WARNINGS

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if sensitivity to Rhus Tox 6X, 12X, 30X, 200X or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

USES

INDICATIONS & USAGE SECTION

For the temporary relief of:
• Painful Joints
• Muscle Aches
• Stiffness in Joints

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician

INDICATIONS

OTC - PURPOSE SECTION

Painful Joints, Muscle Aches, Stiffness in Joints

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Lactose, Magnesium stearate

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Each tablet contains equal parts of Rhus Tox 6X, 12X, 30X, 200X.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hendel Rhus Tox

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62795-1127-2	Hendel Rhus Tox	100 in 1 BOTTLE	TABLET	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62795-1127	HENDEL RHUS TOX (TOXICODENDRON PUBESCENS LEAF) TABLET [MEDINATURA INC]	2	Current NDC, Legacy NDC, 1 package rows	20220823_541a7e75-a464-4fc3-ab75-dc95cab2bbab.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62795-1127-2	EA - Each	62795-1127	e988b3d9-cc51-4978-b4a4-848b1646062e	1	2018-11-06

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Hendel Rhus Tox
TOXICODENDRON PUBESCENS LEAF
MAGNESIUM STEARATE
LACTOSE MONOHYDRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62795-1127	62795-1127-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TOXICODENDRON PUBESCENS LEAF	6IO182RP7A	ACTIB
MAGNESIUM STEARATE	70097M6I30	IACT
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hendel Rhus Tox	TOXICODENDRON PUBESCENS LEAF	MediNatura Inc	541a7e75-a464-4fc3-ab75-dc95cab2bbab	2022-08-22	Warnings	Exact identifier ndc (package): 62795-1127-2 ndc (product): 62795-1127 ndc11 (package): 62795112702 spl id: 1d395e50-5530-43f8-b384-c3081051bfd2 spl set id: 541a7e75-a464-4fc3-ab75-dc95cab2bbab

Reported adverse events (FAERS/openFDA)#

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