Rhumatol

Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia (alba), Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Ledum Palustre, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla (pratensis), Rhododendron Chrysanthum, Rhus Tox, Ruta Graveolens, Salicylicum Acidum, Sepia, Zincum Metallicumk

Hellolife, Inc.
Human Otc Drug
NDC 49726-045

Rhumatol also known as Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia (alba), Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Ledum Palustre, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla (pratensis), Rhododendron Chrysanthum, Rhus Tox, Ruta Graveolens, Salicylicum Acidum, Sepia, Zincum Metallicumk is a human otc drug labeled by 'Hellolife, Inc.'. National Drug Code (NDC) number for Rhumatol is 49726-045. This drug is available in dosage form of Tablet. The names of the active, medicinal ingredients in Rhumatol drug includes Actaea Spicata Root - 10 [hp_X]/1 Anemone Pratensis - 10 [hp_X]/1 Arnica Montana - 10 [hp_X]/1 Bellis Perennis - 10 [hp_X]/1 Black Cohosh - 10 [hp_X]/1 Bryonia Alba Root - 10 [hp_X]/1 Calcium Fluoride - 10 [hp_X]/1 Causticum - 10 [hp_X]/1 Formic Acid - 10 [hp_X]/1 Horse Chestnut - 10 [hp_X]/1 and more. The currest status of Rhumatol drug is Active.

Drug Information:

Drug NDC:	49726-045
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Rhumatol
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia (alba), Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Ledum Palustre, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla (pratensis), Rhododendron Chrysanthum, Rhus Tox, Ruta Graveolens, Salicylicum Acidum, Sepia, Zincum Metallicumk
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Hellolife, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Tablet
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ACTAEA SPICATA ROOT - 10 [hp_X]/1 ANEMONE PRATENSIS - 10 [hp_X]/1 ARNICA MONTANA - 10 [hp_X]/1 BELLIS PERENNIS - 10 [hp_X]/1 BLACK COHOSH - 10 [hp_X]/1 BRYONIA ALBA ROOT - 10 [hp_X]/1 CALCIUM FLUORIDE - 10 [hp_X]/1 CAUSTICUM - 10 [hp_X]/1 FORMIC ACID - 10 [hp_X]/1 HORSE CHESTNUT - 10 [hp_X]/1 Load more... HYPERICUM PERFORATUM - 10 [hp_X]/1 LITHIUM CARBONATE - 10 [hp_X]/1 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE - 10 [hp_X]/1 OYSTER SHELL CALCIUM CARBONATE, CRUDE - 10 [hp_X]/1 PHOSPHORUS - 10 [hp_X]/1 PHYTOLACCA AMERICANA ROOT - 10 [hp_X]/1 RHODODENDRON AUREUM LEAF - 10 [hp_X]/1 RHODODENDRON TOMENTOSUM LEAFY TWIG - 10 [hp_X]/1 RUTA GRAVEOLENS FLOWERING TOP - 10 [hp_X]/1 SALICYLIC ACID - 10 [hp_X]/1 SEPIA OFFICINALIS JUICE - 10 [hp_X]/1 TOXICODENDRON PUBESCENS LEAF - 10 [hp_X]/1 ZINC - 10 [hp_X]/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date:	23 Jul, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	23 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	HelloLife, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UNII:	3FU86L9OS0 8E272251DI O80TY208ZW 2HU33I03UY K73E24S6X9 T7J046YI2B O3B55K4YKI DD5FO1WKFU 0YIW783RG1 3C18L6RJAZ Load more... XK4IUX8MNB 2BMD2GNA4V HF539G9L3Q 2E32821G6I 27YLU75U4W 11E6VI8VEG IV92NQJ73U 877L01IZ0P N94C2U587S O414PZ4LPZ QDL83WN8C2 6IO182RP7A J41CSQ7QDS
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:	Calculi Dissolution Agent [EPC] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Inhibition Small Intestine Fluid/Electrolyte Absorption [PE] Magnesium Ion Exchange Activity [MoA] Mood Stabilizer [EPC] Osmotic Activity [MoA] Osmotic Laxative [EPC] Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
49726-045-60	60 TABLET in 1 BOTTLE, PLASTIC (49726-045-60)	23 Jul, 2019	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Rhumatol

Actaea Spicata & more..

Tablet
HelloLife, Inc.
NDC: 49726-045

Purpose:

Indications for use: for the temporary relief of symptoms such as: â¢ pain â¢ inflammation â¢ stiffness â¢ swelling â¢ weakness product indications are based solely on homeopathic materia medica and have not been evaluated by the fda.

Product Elements:

Rhumatol actaea spicata, aesculus hippocastanum, arnica montana, bellis perennis, bryonia (alba), calcarea carbonica, calcarea fluorica, causticum, cimicifuga racemosa, formicum acidum, ledum palustre, lithium carbonicum, magnesia phosphorica, phosphorus, phytolacca decandra, pulsatilla (pratensis), rhododendron chrysanthum, rhus tox, ruta graveolens, salicylicum acidum, sepia, zincum metallicumk anemone pratensis anemone pratensis rhododendron aureum leaf rhododendron aureum leaf toxicodendron pubescens leaf toxicodendron pubescens leaf ruta graveolens flowering top ruta graveolens flowering top salicylic acid salicylic acid sepia officinalis juice sepia officinalis juice zinc zinc sorbitol silicon dioxide crospovidone copovidone k25-31 lactose monohydrate magnesium stearate mannitol microcrystalline cellulose actaea spicata root actaea spicata root horse chestnut horse chestnut arnica montana arnica montana calcium fluoride fluoride ion bellis perennis bellis perennis bryonia alba root bryonia alba root oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude causticum causticum black cohosh black cohosh formic acid formic acid hypericum perforatum hypericum perforatum rhododendron tomentosum leafy twig ledum palustre twig lithium carbonate lithium cation magnesium phosphate, dibasic trihydrate magnesium cation phosphorus phosphorus phytolacca americana root phytolacca americana root h

Indications and Usage:

Warnings:

Warnings: 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.

Dosage and Administration:

Package Label Principal Display Panel:

Package label display: ndc 49726-045-60 rheumatol tablets natural relief for joint & mobility pain symptoms homeopathic (otc) medicine 60 quick-dissolving tablets rheumatol

Further Questions:

Questions: dist. by: hellolife, inc. 4635 40th st se grand rapids, mi 49512 www.hellolife.net

Comments/ Reviews:

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