Celeragesic

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2024-10-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:28:20

Label at a glance#

ProductCeleragesic
Active ingredientECHINACEA ANGUSTIFOLIA WHOLE, CALENDULA OFFICINALIS FLOWERING TOP, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ECHINACEA PURPUREA WHOLE, BELLIS PERENNIS WHOLE, MATRICARIA CHAMOMILLA WHOLE, HYPERICUM PERFORATUM WHOLE, ACHILLEA MILLEFOLIUM WHOLE, RHODODENDRON TOMENTOSUM LEAFY TWIG, ARNICA MONTANA WHOLE, BRYONIA ALBA ROOT, CALCIUM SULFIDE, NADIDE, PANTOTHENIC ACID, LACTIC ACID, L-, COMFREY ROOT, TOXICODENDRON PUBESCENS LEAF, ACONITUM NAPELLUS WHOLE, SUS SCROFA UMBILICAL CORD, SUS SCROFA ADRENAL GLAND
Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • muscular pain • joint pain • bruising • sports injury These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Aconitum Napellus 12X, Arnica Montana 4X, 12X, 30X, 200X, Bellis Perennis 2X, 6X, Bryonia (Alba) 8X, Calendula Officinalis 1X, 6X, Chamomilla 3X, Echinacea (Angustifolia) 1X, Echinacea Purpurea 2X, Funiculus Umbilicalis Suis 12X, Glandula Suprarenalis Suis 12X, Hamamelis Virginiana 1X, 6X, Hepar Sulphuris Calcareum 8X, Hypericum Perforatum 6X, Ledum Palustre 4X, 6X, Millefolium 3X, 6X, Nadidum 8X, Pantothenic Acid 8X, Rhus Tox 8X, 12X 30X, Sarcolacticum Acidum 8X, Symphytum Officinale 8X.

PURPOSE:

OTC - PURPOSE SECTION

Aconitum Napellus – Muscular Pain, Arnica Montana – Joint Pain, Bellis Perennis - Sports Injury, Bryonia (Alba) - Bruising, Calendula Officinalis – Muscular Pain, Chamomilla – Joint Pain, Echinacea (Angustifolia) – Sports Injury, Echinacea Purpurea – Joint Pain, Funiculus Umbilicalis Suis - Bruising, Glandula Suprarenalis Suis - Bruising, Hamamelis Virginiana – Muscular Pain, Hepar Sulphuris Calcareum – Joint Pain, Hypericum Perforatum – Sports Injury, Ledum Palustre - Bruising, Millefolium – Muscular Pain, Nadidum – Sports Injury, Pantothenic Acid – Joint Pain, Rhus Tox - Bruising, Sarcolacticum Acidum – Muscular Pain, Symphytum Officinale – Sports Injury

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• muscular pain • joint pain • bruising • sports injury

These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

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

Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional.
Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc. 
469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

800-827-8204

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DesBio

Celeragesic

Homeopathic
NDC 43742-1267-1

1 FL OZ (30 ml)

CeleragesicCeleragesic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1267-1Celeragesic30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1267CELERAGESIC (ECHINACEA (ANGUSTIFOLIA), CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, ECHINACEA PURPUREA, BELLIS PERENNIS, CHAMOMILLA, HYPERICUM PERFORATUM, MILLEFOLIUM, LEDUM PALUSTRE, ARNICA MONTANA, BRYONIA (ALBA), HEPAR SULPHURIS CALCAREUM, NADIDUM, PANTOTHENIC ACID, SARCOLACTICUM ACIDUM, SYMPHYTUM OFFICINALE, RHUS TOX, ACONITUM NAPELLUS, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS) LIQUID [DESERET BIOLOGICALS, INC.]3Current NDC, Legacy NDC, 1 package rows20241024_d3d8a7f4-169c-4780-852d-c96a4772e7e3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-126743742-1267-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CeleragesicECHINACEA (ANGUSTIFOLIA), CALENDULA OFFICINALIS, HAMAMELIS VIRGINIANA, ECHINACEA PURPUREA, BELLIS PERENNIS, CHAMOMILLA, HYPERICUM PERFORATUM, MILLEFOLIUM, LEDUM PALUSTRE, ARNICA MONTANA, BRYONIA (ALBA), HEPAR SULPHURIS CALCAREUM, NADIDUM, PANTOTHENIC ACID, SARCOLACTICUM ACIDUM, SYMPHYTUM OFFICINALE, RHUS TOX, ACONITUM NAPELLUS, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUISDeseret Biologicals, Inc.d3d8a7f4-169c-4780-852d-c96a4772e7e32024-10-22WarningsExact identifier
ndc (package): 43742-1267-1
ndc (product): 43742-1267
ndc11 (package): 43742126701
spl id: 8b73b96a-9f1a-4c60-8ddc-51db1fa2c028
spl set id: d3d8a7f4-169c-4780-852d-c96a4772e7e3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.