NDC 57955-2790 Aversion To Exertion

Adrenalinum, Agaricus Muscarius, Aloe Socotrina, Bovista, Calcarea Carbonica, Carpinus Betulus, Flos, Chelidonium Majus, Cocculus Indicus, Helonias Dioica, Hydrofluoricum Acidum, Kali Phosphoricum, Mimosa Pudica, Rosmarinus Officinalis, Sulphur, Tanacetum Vulgare, Taraxacum Officinale, Tropaeolum Majus

NDC Product Code 57955-2790

NDC Code: 57955-2790

Proprietary Name: Aversion To Exertion 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: Adrenalinum, Agaricus Muscarius, Aloe Socotrina, Bovista, Calcarea Carbonica, Carpinus Betulus, Flos, Chelidonium Majus, Cocculus Indicus, Helonias Dioica, Hydrofluoricum Acidum, Kali Phosphoricum, Mimosa Pudica, Rosmarinus Officinalis, Sulphur, Tanacetum Vulgare, Taraxacum Officinale, Tropaeolum Majus 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.


Code Structure
  • 57955 - King Bio Inc.
    • 57955-2790 - Aversion To Exertion

NDC 57955-2790-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

NDC Product Information

Aversion To Exertion with NDC 57955-2790 is a a human over the counter drug product labeled by King Bio Inc.. The generic name of Aversion To Exertion is adrenalinum, agaricus muscarius, aloe socotrina, bovista, calcarea carbonica, carpinus betulus, flos, chelidonium majus, cocculus indicus, helonias dioica, hydrofluoricum acidum, kali phosphoricum, mimosa pudica, rosmarinus officinalis, sulphur, tanacetum vulgare, taraxacum officinale, tropaeolum majus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: King Bio Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.


Aversion To Exertion 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.

  • EPINEPHRINE 10 [hp_X]/59mL
  • AMANITA MUSCARIA FRUITING BODY 10 [hp_X]/59mL
  • ALOE 10 [hp_X]/59mL
  • LYCOPERDON UTRIFORME FRUITING BODY 10 [hp_X]/59mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/59mL
  • CARPINUS BETULUS FLOWERING TOP 10 [hp_X]/59mL
  • CHELIDONIUM MAJUS 10 [hp_X]/59mL
  • ANAMIRTA COCCULUS SEED 10 [hp_X]/59mL
  • CHAMAELIRIUM LUTEUM ROOT 10 [hp_X]/59mL
  • HYDROFLUORIC ACID 10 [hp_X]/59mL
  • POTASSIUM PHOSPHATE, DIBASIC 10 [hp_X]/59mL
  • MIMOSA PUDICA LEAF 10 [hp_X]/59mL
  • ROSMARINUS OFFICINALIS FLOWERING TOP 10 [hp_X]/59mL
  • SULFUR 10 [hp_X]/59mL
  • TANACETUM VULGARE TOP 10 [hp_X]/59mL
  • TARAXACUM OFFICINALE 10 [hp_X]/59mL
  • TROPAEOLUM MAJUS 10 [hp_X]/59mL

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)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

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.

* Please review the disclaimer below.

Aversion To Exertion Product Label Images

Aversion To Exertion 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

Otc - Active Ingredient

Drug Facts___________________________________________________________________________________________________________________HPUS active ingredients: Adrenalinum, Agaricus muscarius, Aloe socotrina, Bovista, Calcarea carbonica, Carpinus betulus, flos, Chelidonium majus, Cocculus indicus, Helonias dioica, Hydrofluoricum acidum, Kali phosphoricum, Mimosa pudica, Rosmarinus officinalis, Sulphur, Tanacetum vulgare, Taraxacum officinale, Tropaeolum majus. Equal volumes of each ingredient in 10X, 30X, 100X, 1LM, 2LM, 3LM, 5LM potencies.

Indications & Usage

Uses a natural aid for: aversion to work, aversion to mental and/or physical exertion, languor, lack of will power, despondency about business.

Inactive Ingredient

Inactive ingredients: Bio-Energetically Enhanced™ pure water, citric acid, potassium sorbate.

Warnings

  • WarningsStop use and ask your doctor if symptoms persist or worsen.If pregnant or breast-feeding, take only on advice of a healthcare professional.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Dosage & Administration

  • DirectionsInitially, depress pump until primed.Spray one dose directly into mouth.Adults: 3 sprays 3 times per day.Children 2-12 years: 2 sprays 3 times per day.Use additionally as needed, up to 6 times per day.

Other Safety Information

Tamper resistant for your protection. Use only if safety seal is intact. This product has not been clinically tested.

Otc - Purpose

  • Use a natural aid for:aversion to workaversion to mental and/or physical exertionlanguorlack of will powerdespondency about business

* Please review the disclaimer below.

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