NDC 61300-0001 Max

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

NDC Product Code 61300-0001

NDC CODE: 61300-0001

Proprietary Name: Max What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Abrotanum (artemisia Abrotanum), Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Graphites, Helleborus Niger, What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 61300 - Arize Supplements, Llc

NDC 61300-0001-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Max with NDC 61300-0001 is a a human over the counter drug product labeled by Arize Supplements, Llc. The generic name of Max is abrotanum (artemisia abrotanum), anacardium orientale, baryta muriatica, calcarea carbonica, calcarea phosphorica, fucus vesiculosus, graphites, helleborus niger, . The product's dosage form is spray and is administered via oral form.

Labeler Name: Arize Supplements, Llc

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Max Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ARTEMISIA ABROTANUM FLOWERING TOP 8 [hp_X]/mL
  • SEMECARPUS ANACARDIUM JUICE 8 [hp_X]/mL
  • BARIUM CHLORIDE DIHYDRATE 8 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 8 [hp_X]/mL
  • FUCUS VESICULOSUS 8 [hp_X]/mL
  • GRAPHITE 8 [hp_X]/mL
  • HELLEBORUS NIGER ROOT 8 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • STRYCHNOS IGNATII SEED 8 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 8 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 8 [hp_X]/mL
  • CLAVICEPS PURPUREA SCLEROTIUM 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • THYMOL 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • ONION 8 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • SUS SCROFA PANCREAS 8 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • MELATONIN 8 [hp_X]/mL
  • NIACINAMIDE 8 [hp_X]/mL
  • SUS SCROFA OVARY 8 [hp_X]/mL
  • SUS SCROFA TESTICLE 8 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 8 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 8 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Arize Supplements, Llc
Labeler Code: 61300
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 04-30-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 07-11-2023 What is the End Marketing Date?
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.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Max Product Label Images

Max Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Abrotanum (Aremisia abrotanum) 8X, Anacardium orientale 8X, Baryta muriatica 8X, Calcarea carbonica 8X, Calcarea phosphorica 8X, Fucus vesiculosus 8X, Graphites 8X, Helleborus niger 8X, Hypothalamus (suis) 8X, Ignatia amara 8X, Lycopodium clavatum 8X, Magnesia phosphorica 8X, Secale cornutum 8X, Silicea 8X, Thymolum 8X, Thyroidinum (suis) 8X, Allium cepa 8X, 2X, 16X, Hepar suis 8X, 12X, 16X, Pancreas suis 8X, 12X, 16X, Glandula suprarenalis suis 8X, 12X, 16X, Melatonin 8X, 32C, Nicotinamidum 8X, 32C, Oophorinum (suis) 8X, 32C, Orchitinum (suis) 8X, 32C, Serotonin (hydrochloride) 8X, 32C, Thiaminum hydrochloricum 8X, 32C, Solidago virgaurea 12X.

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.

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.

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.

Keep Out Of Reach Of Children:

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

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.

Inactive Ingredients:

Demineralized water, 20% Ethanol

Questions:

Distributed by:ARIZE Supplements, LLC400 Whitesport Dr SW, Suite 101, Huntsville, AL 25801

Package Label Display

NDC 61300-0001-1ARIZE CLINICMaximize Your Weight Health JourneyMAXWEIGHT LOOS AND APPETITE CONTROLProprietary Homeopathic RemedyFor Professional Use Only20% Ethanol1 FL. OZ. (30 ml)

* Please review the disclaimer below.