NDC 43742-0847 Celeragesic

Echinacea (angustifolia), Calendula Officinalis, Hamamelis Virginiana, Echinacea Purpurea, Bellis Perennis, Aconitum Napellus, Chamomilla, Hypericum Perforatum, Belladonna, Millefolium, Bryonia (alba), Arnica Montana, Rhus Tox, Adenosinum Triphosphoricum Dinatrum, Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Hepar Sulphuris Calcareum, Impatiens Glandulifera, Flos, Mercurius Solubilis, Nadidum, Ornithogalum Umbellatum, Flos, Pantothenic Acid, Prunus Cerasifera, Flos, Sarcolacticum Acidum

NDC Product Code 43742-0847

NDC Code: 43742-0847

Proprietary Name: Celeragesic 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: Echinacea (angustifolia), Calendula Officinalis, Hamamelis Virginiana, Echinacea Purpurea, Bellis Perennis, Aconitum Napellus, Chamomilla, Hypericum Perforatum, Belladonna, Millefolium, Bryonia (alba), Arnica Montana, Rhus Tox, Adenosinum Triphosphoricum Dinatrum, Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Hepar Sulphuris Calcareum, Impatiens Glandulifera, Flos, Mercurius Solubilis, Nadidum, Ornithogalum Umbellatum, Flos, Pantothenic Acid, Prunus Cerasifera, Flos, Sarcolacticum Acidum 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

  • 43742 - Deseret Biologicals, Inc.
    • 43742-0847 - Celeragesic

NDC 43742-0847-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Celeragesic with NDC 43742-0847 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Celeragesic is echinacea (angustifolia), calendula officinalis, hamamelis virginiana, echinacea purpurea, bellis perennis, aconitum napellus, chamomilla, hypericum perforatum, belladonna, millefolium, bryonia (alba), arnica montana, rhus tox, adenosinum triphosphoricum dinatrum, clematis vitalba, flos, helianthemum nummularium, flos, hepar sulphuris calcareum, impatiens glandulifera, flos, mercurius solubilis, nadidum, ornithogalum umbellatum, flos, pantothenic acid, prunus cerasifera, flos, sarcolacticum acidum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, 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.

Celeragesic 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.

  • ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL
  • CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/mL
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 1 [hp_X]/mL
  • ECHINACEA PURPUREA 2 [hp_X]/mL
  • BELLIS PERENNIS 2 [hp_X]/mL
  • ACONITUM NAPELLUS 3 [hp_X]/mL
  • MATRICARIA RECUTITA 3 [hp_X]/mL
  • HYPERICUM PERFORATUM 3 [hp_X]/mL
  • ATROPA BELLADONNA 3 [hp_X]/mL
  • ACHILLEA MILLEFOLIUM 3 [hp_X]/mL
  • BRYONIA ALBA ROOT 4 [hp_X]/mL
  • ARNICA MONTANA 4 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 8 [hp_X]/mL
  • CLEMATIS VITALBA FLOWER 8 [hp_X]/mL
  • HELIANTHEMUM NUMMULARIUM FLOWER 8 [hp_X]/mL
  • CALCIUM SULFIDE 8 [hp_X]/mL
  • IMPATIENS GLANDULIFERA FLOWER 8 [hp_X]/mL
  • MERCURIUS SOLUBILIS 8 [hp_X]/mL
  • NADIDE 8 [hp_X]/mL
  • ORNITHOGALUM UMBELLATUM FLOWERING TOP 8 [hp_X]/mL
  • PANTOTHENIC ACID 8 [hp_X]/mL
  • PRUNUS CERASIFERA FLOWER 8 [hp_X]/mL
  • LACTIC ACID, L- 8 [hp_X]/mL
  • COMFREY ROOT 8 [hp_X]/mL
  • UBIDECARENONE 8 [hp_X]/mL
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 12 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 12 [hp_X]/mL
  • SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS 12 [hp_X]/mL
  • PROTEUS MORGANII 30 [hp_C]/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: Deseret Biologicals, Inc.
Labeler Code: 43742
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: 09-15-2016 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: 12-20-2021 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Celeragesic Product Label Images

Celeragesic 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:

Echinacea (Angustifolia) 1X, Calendula Officinalis 1X, 6X, Hamamelis Virginiana 1X, 6X, Echinacea Purpurea 2X, Bellis Perennis 2X, 6X, Aconitum Napellus 3X, Chamomilla 3X, Hypericum Perforatum 3X, Belladonna 3X, 6X, Millefolium 3X, 6X, Bryonia (Alba) 4X, Arnica Montana 4X,12X, 30X, 200X, Rhus Tox 6X, 12X, 30X, Adenosinum Triphosphoricum Dinatrum 8X, Clematis Vitalba, Flos 8X, Helianthemum Nummularium, Flos 8X, Hepar Sulphuris Calcareum 8X, Impatiens Glandulifera, Flos 8X, Mercurius Solubilis 8X, Nadidum 8X, Ornithogalum Umbellatum, Flos 8X, Pantothenic Acid 8X, Prunus Cerasifera, Flos 8X, Sarcolacticum Acidum 8X, Symphytum Officinale 8X, Ubidecarenonum 8X, Carbo Vegetabilis 12X, Funiculus Umbilicalis Suis 12X, Glandula Suprarenalis Suis 12, Thalamus Opticus (Suis) 12X, Proteus (Morgani) 30C.

Indications:

For the temporary relief of muscular pain, joint pain, sports injuries and bruising.

For the temporary relief of muscular pain, joint pain, sports injuries and bruising.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

Directions:

10 drops under the tongue, 3 to 6 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 25% ethanol

Questions:

Dist. By: Deseret Biologicals, Inc. • www.desbio.com469 Parkland Drive  Sandy, UT 84070

Package Label Display:

DESBIONDC 43742-0847-1CELERAGESICHomeopathic Management of Acute Pain1 FL OZ (30 ml)

* Please review the disclaimer below.

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