NDC 57955-2311 Calloused

Allium Sativum, Anacardium Orientale, Calendula Officinalis, Capsicum Annuum, Ceanothus Americanus, Chamomilla, Chelidonium Majus, Conium Maculatum, Kali Carbonicum, Lobelia Cardinalis, Mancinella, Myristica Sebifera, Pinus Sylvestris, Flos, Stigmata Maidis, Sepia, Taraxacum Officinale, Thea Sinensis

NDC Product Code 57955-2311

NDC Code: 57955-2311

Proprietary Name: Calloused 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: Allium Sativum, Anacardium Orientale, Calendula Officinalis, Capsicum Annuum, Ceanothus Americanus, Chamomilla, Chelidonium Majus, Conium Maculatum, Kali Carbonicum, Lobelia Cardinalis, Mancinella, Myristica Sebifera, Pinus Sylvestris, Flos, Stigmata Maidis, Sepia, Taraxacum Officinale, Thea Sinensis 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.
    • 57955-2311 - Calloused

NDC 57955-2311-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

NDC Product Information

Calloused with NDC 57955-2311 is a a human over the counter drug product labeled by King Bio Inc.. The generic name of Calloused is allium sativum, anacardium orientale, calendula officinalis, capsicum annuum, ceanothus americanus, chamomilla, chelidonium majus, conium maculatum, kali carbonicum, lobelia cardinalis, mancinella, myristica sebifera, pinus sylvestris, flos, stigmata maidis, sepia, taraxacum officinale, thea sinensis. 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.


Calloused 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.

  • GARLIC 10 [hp_X]/59mL
  • SEMECARPUS ANACARDIUM JUICE 10 [hp_X]/59mL
  • CALENDULA OFFICINALIS FLOWERING TOP 10 [hp_X]/59mL
  • CAPSICUM 10 [hp_X]/59mL
  • CEANOTHUS AMERICANUS LEAF 10 [hp_X]/59mL
  • MATRICARIA RECUTITA 10 [hp_X]/59mL
  • CHELIDONIUM MAJUS 10 [hp_X]/59mL
  • CONIUM MACULATUM FLOWERING TOP 10 [hp_X]/59mL
  • POTASSIUM CARBONATE 10 [hp_X]/59mL
  • LOBELIA CARDINALIS 10 [hp_X]/59mL
  • HIPPOMANE MANCINELLA FRUITING LEAFY TWIG 10 [hp_X]/59mL
  • VIROLA SEBIFERA RESIN 10 [hp_X]/59mL
  • PINUS SYLVESTRIS FLOWERING TOP 10 [hp_X]/59mL
  • CORN SILK 10 [hp_X]/59mL
  • SEPIA OFFICINALIS JUICE 10 [hp_X]/59mL
  • TARAXACUM OFFICINALE 10 [hp_X]/59mL
  • GREEN TEA LEAF 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)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • 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.

Calloused Product Label Images

Calloused 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 activeingredients: Allium sativum, Anacardium orientale, Calendula officinalis, Capsicum annuum, Ceanothus americanus, Chamomilla, Chelidonium majus, Conium maculatum, Kali carbonicum, Lobelia cardinalis, Mancinella, Myristica sebifera, Pinus sylvestris, flos, Stigmata maidis, Sepia, Taraxacum officinale, Thea sinensis. Equal volumes of each ingredient in 10X, 30X, 100X, LM1, LM2, LM3, LM5 potencies.

Indications & Usage

Uses for temporary relief of: hard-heartedness, fear of losing control. indifference, coldness toward others.

Inactive Ingredient

Inactive Ingredients:Bio-Energetically Enhanced™ pure water, citric acid and 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: 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.

Otc - Purpose

  • Uses ​for temporary relief of:hard-heartednessfear of losing controlindifferencecoldness toward others

* Please review the disclaimer below.

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