Oratox

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2024-10-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:28:22

Label at a glance#

ProductOratox
Active ingredientFUCUS VESICULOSUS, SUS SCROFA LYMPH, SUS SCROFA BONE MARROW, SUS SCROFA THYMUS, THYROID, CALCIUM CHLORIDE, IODINE, SODIUM FLUORIDE, SODIUM CHLORIDE, SELENIUM, VANADIUM, SILVER, GOLD, COPPER, EUGENOL, FORMALDEHYDE, LIDOCAINE, MERCURIUS SOLUBILIS, MOLYBDENUM, NICKEL, PALLADIUM, TIN, TITANIUM, ZINC
Label structure9 sections

Indications and uses

• For the temporary relief of symptoms including: • muscle cramps • inflammation • joint pain 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, 2 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

Argentum Metallicum 12X, 30X, 60X, 200X, Aurum Metallicum 12X, 30X, 60X, 200X, Calcarea Muriatica 12X, Cuprum Metallicum 12X, 30X, 60X, 200X, Eugenol 12X, 30X, 60X, 200X, Formalinum 12X, 30X, 60X, 200X, Fucus Vesiculosus 3X, Iodium 12X, Lidocaine 12X, 30X, 60X, 200X, Lymph Node (Suis) 8X, Medulla Ossis Suis 8X, Mercurius Solubilis 12X, 30X, 60X, 200X, Molybdenum 12X, 30X, 60X, 200X, Natrum Fluoratum 12X, Natrum Muriaticum 12X, Niccolum Metallicum 12X, 30X, 60X, 200X, Palladium Metallicum 12X, 30X, 60X, 200X, Selenium Metallicum 12X, Stannum Metallicum 12X, 30X, 60X, 200X, Thyroidinum (Suis) 8X, Thymus (Suis) 8X, Titanium Metallicum 12X, 30X, 60X, 200X, Vanadium Metallicum 12X, Zincum Metallicum 12X, 30X, 60X, 200X.

PURPOSE:

OTC - PURPOSE SECTION

Argentum Metallicum – Muscle Cramps, Aurum Metallicum - Inflammation, Calcarea Muriatica – Joint Pain, Cuprum Metallicum – Muscle Cramps, Eugenol - Inflammation, Formalinum - Inflammation, Fucus Vesiculosus – Joint Pain, Iodium - Inflammation, Lidocaine – Joint Pain, Lymph Node (Suis) - Inflammation, Medulla Ossis Suis – Muscle Cramps, Mercurius Solubilis – Joint Pain, Molybdenum – Muscle Cramps, Natrum Fluoratum - Inflammation, Natrum Muriaticum – Joint Pain, Niccolum Metallicum - Inflammation, Palladium Metallicum - Inflammation, Selenium Metallicum – Joint Pain, Stannum Metallicum – Muscle Cramps, Thyroidinum (Suis) - Inflammation, Thymus (Suis) - Inflammation, Titanium Metallicum – Muscle Cramps, Vanadium Metallicum - Inflammation, Zincum Metallicum – Joint Pain

USES:

INDICATIONS & USAGE SECTION

• For the temporary relief of symptoms including:

• muscle cramps • inflammation • joint pain

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, 2 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

Oratox

Homeopathic

NDC 43742-0944-1

1 FL OZ (30 ml)

OratoxOratox

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-0944-1Oratox30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-0944ORATOX (FUCUS VESICULOSUS, LYMPH NODE (SUIS), MEDULLA OSSIS SUIS, THYMUS (SUIS), THYROIDINUM (SUIS), CALCAREA MURIATICA, IODIUM, NATRUM FLUORATUM, NATRUM MURIATICUM, SELENIUM METALLICUM, VANADIUM METALLICUM, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, EUGENOL, FORMALINUM, LIDOCAINE, MERCURIUS SOLUBILIS, MOLYBDENUM METALLICUM, NICCOLUM METALLICUM, PALLADIUM METALLICUM, STANNUM METALLICUM, TITANIUM METALLICUM, ZINCUM METALLICUM) LIQUID [DESERET BIOLOGICALS, INC.]4Current NDC, Legacy NDC, 1 package rows20241025_b78d8991-ffbe-4b11-b9b9-8fe432bed8aa.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-094443742-0944-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 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
OratoxFUCUS VESICULOSUS, LYMPH NODE (SUIS), MEDULLA OSSIS SUIS, THYMUS (SUIS), THYROIDINUM (SUIS), CALCAREA MURIATICA, IODIUM, NATRUM FLUORATUM, NATRUM MURIATICUM, SELENIUM METALLICUM, VANADIUM METALLICUM, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, EUGENOL, FORMALINUM, LIDOCAINE, MERCURIUS SOLUBILIS, MOLYBDENUM METALLICUM, NICCOLUM METALLICUM, PALLADIUM METALLICUM, STANNUM METALLICUM, TITANIUM METALLICUM, ZINCUM METALLICUMDeseret Biologicals, Inc.b78d8991-ffbe-4b11-b9b9-8fe432bed8aa2024-10-23WarningsExact identifier
ndc (package): 43742-0944-1
ndc (product): 43742-0944
ndc11 (package): 43742094401
spl id: f735ac6a-9396-4f30-8139-8afbaf56c87f
spl set id: b78d8991-ffbe-4b11-b9b9-8fe432bed8aa

Reported adverse events (FAERS/openFDA)#

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