Max

Abrotanum (artemisia Abrotanum), Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Graphites, Helleborus Niger,

Arize Supplements, Llc
Human Otc Drug
NDC 61300-0001

Max also known as Abrotanum (artemisia Abrotanum), Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Graphites, Helleborus Niger, is a human otc drug labeled by 'Arize Supplements, Llc'. National Drug Code (NDC) number for Max is 61300-0001. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Max drug includes Artemisia Abrotanum Flowering Top - 8 [hp_X]/mL Barium Chloride Dihydrate - 8 [hp_X]/mL Claviceps Purpurea Sclerotium - 8 [hp_X]/mL Fucus Vesiculosus - 8 [hp_X]/mL Graphite - 8 [hp_X]/mL Helleborus Niger Root - 8 [hp_X]/mL Lycopodium Clavatum Spore - 8 [hp_X]/mL Magnesium Phosphate, Dibasic Trihydrate - 8 [hp_X]/mL Melatonin - 8 [hp_X]/mL Niacinamide - 8 [hp_X]/mL and more. The currest status of Max drug is Active.

Drug Information:

Drug NDC:	61300-0001
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:	Max
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:	Abrotanum (artemisia Abrotanum), Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Graphites, Helleborus Niger,
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Arize Supplements, Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Spray
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:	ARTEMISIA ABROTANUM FLOWERING TOP - 8 [hp_X]/mL BARIUM CHLORIDE DIHYDRATE - 8 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM - 8 [hp_X]/mL FUCUS VESICULOSUS - 8 [hp_X]/mL GRAPHITE - 8 [hp_X]/mL HELLEBORUS NIGER ROOT - 8 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 8 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE - 8 [hp_X]/mL MELATONIN - 8 [hp_X]/mL NIACINAMIDE - 8 [hp_X]/mL Load more... ONION - 8 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 8 [hp_X]/mL PORK LIVER - 8 [hp_X]/mL SEMECARPUS ANACARDIUM JUICE - 8 [hp_X]/mL SEROTONIN HYDROCHLORIDE - 8 [hp_X]/mL SILICON DIOXIDE - 8 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP - 12 [hp_X]/mL STRYCHNOS IGNATII SEED - 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 8 [hp_X]/mL SUS SCROFA HYPOTHALAMUS - 8 [hp_X]/mL SUS SCROFA OVARY - 8 [hp_X]/mL SUS SCROFA PANCREAS - 8 [hp_X]/mL SUS SCROFA TESTICLE - 8 [hp_X]/mL SUS SCROFA THYROID - 8 [hp_X]/mL THIAMINE HYDROCHLORIDE - 8 [hp_X]/mL THYMOL - 8 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE - 8 [hp_X]/mL
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:	30 Apr, 2014
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	11 Jul, 2023
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:	10 Jun, 2026
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:	Arize Supplements, LLC
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.
UPC:	0854508005001
UPC stands for Universal Product Code.
NUI:	N0000185371 N0000175629 N0000184306 M0000728 M0006342 M0022575
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	QG07G580U0 EL5GJ3U77E 01G9XEA93N 535G2ABX9M 4QQN74LH4O 608DGJ6815 C88X29Y479 HF539G9L3Q JL5DK93RCL 25X51I8RD4 Load more... 492225Q21H 2E32821G6I 6EC706HI7F Y0F0BU8RDU GKN429M9VS ETJ7Z6XBU4 5405K23S50 1NM3M2487K 398IYQ16YV N6R0856Z79 S7YTV04R8O 9Y3J3362RY KM02613O28 6RV024OAUQ M572600E5P 3J50XA376E 91D9GV0Z28
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 EPC:	Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Vegetable Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Blood Coagulation Factor [EPC] Calcium [CS] Calculi Dissolution Agent [EPC] Cations Divalent [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Coagulation Factor Activity [PE] Increased Histamine Release [PE] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Inhibition Small Intestine Fluid/Electrolyte Absorption [PE] Magnesium Ion Exchange Activity [MoA] Non-Standardized Food Allergenic Extract [EPC] Osmotic Activity [MoA] Osmotic Laxative [EPC] Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] Vegetable Proteins [CS]
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
61300-0001-1	30 mL in 1 BOTTLE, SPRAY (61300-0001-1)	30 Apr, 2014	11 Jul, 2023	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

Max

Abrotanum (artemisia Abrotanum) & more..

Spray
Arize Supplements, LLC
NDC: 61300-0001

Purpose:

Indications: for temporary relief of symptoms related to increased appetite, cravings, regulation of fat metabolism and detoxification stress. may provide glandular support of the liver, gallbladder, endocrine system and neuro-endocrine metabolism.

Product Elements:

Max abrotanum (artemisia abrotanum), anacardium orientale, baryta muriatica, calcarea carbonica, calcarea phosphorica, fucus vesiculosus, graphites, helleborus niger, artemisia abrotanum flowering top artemisia abrotanum flowering top semecarpus anacardium juice semecarpus anacardium juice barium chloride dihydrate barium cation oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude tribasic calcium phosphate calcium cation fucus vesiculosus fucus vesiculosus graphite graphite helleborus niger root helleborus niger root sus scrofa hypothalamus sus scrofa hypothalamus strychnos ignatii seed strychnos ignatii seed lycopodium clavatum spore lycopodium clavatum spore magnesium phosphate, dibasic trihydrate magnesium cation claviceps purpurea sclerotium claviceps purpurea sclerotium silicon dioxide silicon dioxide thymol thymol sus scrofa thyroid sus scrofa thyroid onion onion pork liver pork liver sus scrofa pancreas sus scrofa pancreas sus scrofa adrenal gland sus scrofa adrenal gland melatonin melatonin niacinamide niacinamide sus scrofa ovary sus scrofa ovary sus scrofa testicle sus scrofa testicle serotonin hydrochloride serotonin thiamine hydrochloride thiamine ion solidago virgaurea flowering top solidago virgaurea flowering top water alcohol

Indications and Usage:

Warnings:

Warnings: stop use if conditions persist or worsen. if pregnant or breast feeding ask a healthcare professional before use. keep out of reach of children. contains alcohol. in case of overdose, get medical help or contact a poison control center right away. other information: do not use if tamper evident seal is broken or missing. store in a cool dry place.

Dosage and Administration:

Directions: swirl or shake bottle vigorously 5-10 times prior to use. apply three sprays under your tongue twice per day, upon awakening and at bedtime. do not eat, drink or brush your teeth within 5-10 minutes before or after taking this product. consult your physician prior to use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display ndc 61300-0001-1 arize clinic maximize your weight health journey max weight loos and appetite control proprietary homeopathic remedy for professional use only 20% ethanol 1 fl. oz. (30 ml) max

Further Questions:

Questions: distributed by: arize supplements, llc 400 whitesport dr sw, suite 101, huntsville, al 25801

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.