NDC 43742-0377 Celeragesic

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

NDC Product Code 43742-0377

NDC Code: 43742-0377

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), Echinacea Purpurea, Bellis Perennis, Calendula Officinalis, Hamamelis Virginiana, Aconitum Napellus, Chamomilla, Hypericum Perforatum, Belladonna, Millefolium, Bryonia (alba), Arnica Montana, Rhus Tox, Adenosinum Triphosphoricum Dinatrum, Clematis Vitalba Flos, Coenzyme A, Helianthemum Nummularium Flos, Hepar Sulphuris Calcareum, Impatiens Glandulifera Flos, Mercurius Solubilis, Nadidum, Ornithogalum Umbellatum Flos, 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.
    • 43742-0377 - Celeragesic

NDC 43742-0377-1

Package Description: 57 g in 1 TUBE

NDC Product Information

Celeragesic with NDC 43742-0377 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Celeragesic is echinacea (angustifolia), echinacea purpurea, bellis perennis, calendula officinalis, hamamelis virginiana, aconitum napellus, chamomilla, hypericum perforatum, belladonna, millefolium, bryonia (alba), arnica montana, rhus tox, adenosinum triphosphoricum dinatrum, clematis vitalba flos, coenzyme a, helianthemum nummularium flos, hepar sulphuris calcareum, impatiens glandulifera flos, mercurius solubilis, nadidum, ornithogalum umbellatum flos, prunus cerasifera, flos, sarcolacticum acidum. The product's dosage form is gel and is administered via topical form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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 2 [hp_X]/g
  • ECHINACEA PURPUREA 2 [hp_X]/g
  • BELLIS PERENNIS 2 [hp_X]/g
  • CALENDULA OFFICINALIS FLOWERING TOP 2 [hp_X]/g
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 2 [hp_X]/g
  • ACONITUM NAPELLUS 3 [hp_X]/g
  • MATRICARIA RECUTITA 3 [hp_X]/g
  • HYPERICUM PERFORATUM 3 [hp_X]/g
  • ATROPA BELLADONNA 3 [hp_X]/g
  • ACHILLEA MILLEFOLIUM 3 [hp_X]/g
  • BRYONIA ALBA ROOT 4 [hp_X]/g
  • ARNICA MONTANA 4 [hp_X]/g
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/g
  • ADENOSINE TRIPHOSPHATE DISODIUM 8 [hp_X]/g
  • CLEMATIS VITALBA FLOWER 8 [hp_X]/g
  • COENZYME A 8 [hp_X]/g
  • HELIANTHEMUM NUMMULARIUM FLOWER 8 [hp_X]/g
  • CALCIUM SULFIDE 8 [hp_X]/g
  • IMPATIENS GLANDULIFERA FLOWER 8 [hp_X]/g
  • MERCURIUS SOLUBILIS 8 [hp_X]/g
  • NADIDE 8 [hp_X]/g
  • ORNITHOGALUM UMBELLATUM 8 [hp_X]/g
  • PRUNUS CERASIFERA FLOWER 8 [hp_X]/g
  • LACTIC ACID, L- 8 [hp_X]/g
  • COMFREY ROOT 8 [hp_X]/g
  • UBIDECARENONE 8 [hp_X]/g
  • ACTIVATED CHARCOAL 12 [hp_X]/g
  • SUS SCROFA UMBILICAL CORD 12 [hp_X]/g
  • SUS SCROFA ADRENAL GLAND 12 [hp_X]/g
  • SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS 12 [hp_X]/g
  • PROTEUS MORGANII 30 [hp_C]/g

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.

  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • OREGANO (UNII: 0E5AT8T16U)
  • POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
  • PEG-8 DIMETHICONE (UNII: GIA7T764OD)
  • POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • SORBIC ACID (UNII: X045WJ989B)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • 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.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

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: 05-12-2014 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: 12-23-2020 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 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) 2X, Echinacea Purpurea 2X, Bellis Perennis 2X, 6X, Calendula Officinalis 2X, 6X, Hamamelis Virginiana 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, Coenzyme A 8X, Helianthemum Nummularium Flos 8X, Hepar Sulphuris Calcareum 8X, Impatiens Glandulifera Flos 8X, Mercurius Solubilis 8X, Nadidum 8X, Ornithogalum Umbellatum Flos 8X, Prunus Cerasifera Flos 8X, Sarcolacticum Acidum 8X, Symphytum Officinale 8X, Ubidecarenonum 8X, Carbo Vegetabilis 12X, Funiculus Umbilicalis Suis 12X, Glandula Suprarenalis Suis 12X, Thalamus Opticus (Suis) 12X, Morgan Bacillus (Pure) 30C.

Homeopathic Indications:

For the temporary relief of muscular pain, joint pain, sports injuries and bruising.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of muscular pain, joint pain, sports injuries and bruising.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

For external use only.Keep out of reach of children.  If swallowed, get medical help or contact 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.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Apply to the affected area as needed.

Inactive Ingredients:

Demineralized Water, Phenoxyethanol, Caprylyl Glycol, Sorbic Acid, Sodium Hydroxide Solution, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, PEG-33, PEG-8 Dimethicone, PEG-14, Aloe Barbadensis Leaf Juice, Tocopherols [Vitamin E Oil], Edate Disodium, Natural plant extract, Potassium Sorbate

Questions:

Dist. By Deseret Biologicals, Inc.www.desbio.com469 W. Parkland DriveSandy, UT 84070

Package Label Display:

DESBIONDC 43742-0377-1CELERAGESICHomeopathic Gel for Management of Acute PainNET WT 2 OZ  (57 g)

* Please review the disclaimer below.

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