BM Rhus Tox Ointment

Manufacturer
BM Private Limited
Effective date
2026-02-12
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:37:34

Label at a glance#

ProductBM Rhus Tox
Active ingredientCINNAMON, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA ALBA ROOT, CAMPHOR (NATURAL), TURMERIC, COLCHICUM AUTUMNALE BULB, TOXICODENDRON PUBESCENS LEAF
Label structure9 sections

Storage and handling

Storage: Store in a cool, dry place below 30°C (86°F). Protect from direct sunlight.

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Cetostearyl alcohol, Paraffin oil, White soft paraffin

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Arnica mont Ø (HPUS)

Bellis per Ø (HPUS)

Bryonia alb D7 (EHPI)

Camphora Ø (HPUS)

Cinnamomum Ø (HPUS)

Colchicum D6 (HPUS)

Curcuma longa Ø (GHP)

Rhus toxicodendron D6 Ø (HPUS)

INDICATIONS & USAGE SECTION

Uses*

Helps temporarily relieve: joint and muscle aches; stiffness; swelling; discomfort; soreness

OTC - PURPOSE SECTION

Active ingredients Purpose*

Arnica mont Ø (HPUS).................joint pain

Bellis per Ø (HPUS)....................soreness & stiffness

Bryonia alb D7 (EHPI)...............joint discomfort

Camphora Ø (HPUS).................soreness

Cinnamomum Ø (HPUS)...........poor circulation

Colchicum D6 (HPUS).............stiffness

Curcuma longa Ø (GHP)...........pain & swelling

Rhus toxicodendron D6 (HPUS).. stiffness and joint & muscle pain

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings:

Keep out of reach of children.

WARNINGS SECTION

Warnings:

For external use only.

Avoid contact with eyes and mucous membranes.

Keep out of reach of children.

If you have severe symptoms, consult a doctor before use.

Do not use on broken or damaged skin.

STORAGE AND HANDLING SECTION

Storage:

Store in a cool, dry place below 30°C (86°F).

Protect from direct sunlight.

DOSAGE & ADMINISTRATION SECTION

Directions:

Use as directed.

Clean the affected area before application.

Apply a thin layer to the affected area, 2-3 times daily or as directed by a physician.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 1:

Rhux ToxRhux Tox

Package 2:

TUBE

RHUS TOX OINTMENT TUBERHUS TOX OINTMENT TUBE

BOX

RHUS BOX OINTMENT BOXRHUS BOX OINTMENT BOX

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR CodeBM Homoeopathic Pharmaceuticals Rhus Tox (Ointment) 40gm Help support to relieve the symptoms of joints pain and stiffness (For external use only) DRAP Mfg. Enl. # 0041, Prod. Enl. # 0041880978Rhus Tox.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-6023-1BM Rhus Tox40 g in 1 JAROINTMENT404
85816-6023-2BM Rhus Tox40 g in 1 TUBEOINTMENT404

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85816-602385816-6023-1, 85816-6023-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-12-03monthly-update2026-06-03 17:44:52
12025-06-27full-release2026-06-01 02:34:12

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
BM Rhus ToxRHUS TOXBM Private Limited3890f0d6-0f02-2266-e063-6394a90ae2bc2026-02-12WarningsExact identifier
ndc (package): 85816-6023-1
ndc (package): 85816-6023-2
ndc (product): 85816-6023
ndc11 (package): 85816602302
ndc11 (package): 85816602301
spl id: 4aa04a61-ac81-e9d1-e063-6394a90a2902
spl set id: 3890f0d6-0f02-2266-e063-6394a90ae2bc

Reported adverse events (FAERS/openFDA)#

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