Rhumatol

Manufacturer
HelloLife, Inc. | Apotheca Company
Effective date
2023-10-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:23:38

Label at a glance#

ProductRhumatol
Active ingredientANEMONE PRATENSIS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, SALICYLIC ACID, SEPIA OFFICINALIS JUICE, ZINC, ACTAEA SPICATA ROOT, HORSE CHESTNUT, ARNICA MONTANA, CALCIUM FLUORIDE, BELLIS PERENNIS, BRYONIA ALBA ROOT, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, BLACK COHOSH, FORMIC ACID, HYPERICUM PERFORATUM, RHODODENDRON TOMENTOSUM LEAFY TWIG, LITHIUM CARBONATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHOSPHORUS, PHYTOLACCA AMERICANA ROOT
Label structure9 sections

Storage and handling

Do not store next to electrical devices or appliances. Keep lid tightly closed & store in a cool, dry place.

Label contents#

Full prescribing information#

ACTIVE HPUS INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Actaea Spicata 10X, 300X, 200C, Aesculus Hippocastanum 10X, 300X, 200C, Arnica Montana 10X, 300X, 200C, Bellis Perennis 10X, 300X, 200C, Bryonia (Alba) 10X, 300X, 200C, Calcarea Carbonica 10X, 300X, 200C, Calcarea Fluorica 10X, 300X, 200C, Causticum 10X, 300X, 200C, Cimicifuga Racemosa 10X, 300X, 200C, Formicum Acidum 10X, 300X, 200C, Ledum Palustre 10X, 300X, 200C, Lithium Carbonicum 10X, 300X, 200C, Magnesia Phosphorica 10X, 300X, 200C, Phosphorus 10X, 300X, 200C, Phytolacca Decandra 10X, 300X, 200C, Pulsatilla (Pratensis) 10X, 300X, 200C, Rhododendron Chrysanthum 10X, 300X, 200C, Rhus Tox 10X, 300X, 200C, Ruta Graveolens 10X, 300X, 200C, Salicylicum Acidum 10X, 300X, 200C, Sepia 10X, 300X, 200C, Zincum Metallicum 10X, 300X, 200C.

INDICATIONS FOR USE:

OTC - PURPOSE SECTION

For the temporary relief of symptoms such as:

• pain

• inflammation

• stiffness

• swelling

• weakness

Product indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA.

WARNINGS:

WARNINGS SECTION

Stop use and as a doctor if symptoms persist or worsen.

If pregnant or breast-feeding, ask a health professional before use.

Do not use if tamper seal is broken.

STORAGE & HANDLING:

STORAGE AND HANDLING SECTION

Do not store next to electrical devices or appliances.

Keep lid tightly closed & store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS FOR USE:

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms such as:

• pain

• inflammation

• stiffness

• swelling

• weakness

Product indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Advantol 300, Lactose, Magnesium Stearate, Mannitol, Microcrystalline Cellulose.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by: HelloLife, Inc.

4635 40th St SE

Grand Rapids, MI 49512

www.hellolife.net

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49726-045-60
RHEUMATOL
TABLETS
Natural Relief for Joint &
Mobility Pain Symptoms
Homeopathic (OTC) Medicine
60 Quick-dissolving Tablets

RheumatolRheumatol

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49726-04549726-045-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
28db8c29-4320-4764-e063-6294a90a45bd2432606f-1569-47cd-9644-9be5860c7fe32024-12-09WarningsExact identifier
spl set id: 2432606f-1569-47cd-9644-9be5860c7fe3

Reported adverse events (FAERS/openFDA)#

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