EMF

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2024-07-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:27:27

Label at a glance#

ProductEMF
Active ingredientSILVER NITRATE, ARNICA MONTANA WHOLE, BAPTISIA TINCTORIA ROOT, CINCHONA OFFICINALIS BARK, GALIUM APARINE WHOLE, PORK LIVER, SODIUM CARBONATE, ASIAN GINSENG, PHOSPHORIC ACID, PHOSPHORUS, RHODODENDRON AUREUM LEAF, STRONTIUM CARBONATE, SULFUR IODIDE, THUJA OCCIDENTALIS LEAFY TWIG, ALCOHOL, X-RAY EXPOSED (1000 RAD)
Label structure9 sections

Indications and uses

May temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (EMF) radiation exposure, such as: recurring fatigue nausea disturbed sleep frequent headaches mental confusion** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

Adults and children over 12:  Spray twice under the tongue three times per day for one month. For the next three months use same dosage one week per month. Children 12 and under:  Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each spray): 6.67% of Argentum nitricum 30C, Arnica montana 3X, Baptisia tinctoria 3X, Cinchona officinalis 6X, Galium aparine 3X, Hepar suis 6X, Natrum carbonicum 200C, Panax ginseng 1X, Phosphorus 12X, Phosphoricum acidum 3X, Rhododendron Chrysanthum 30C, Strontium Carbonicum 12X, Sulphur iodatum 200C, Thuja occidentalis 200C, X-Ray 200C.

USES:

OTC - PURPOSE SECTION

May temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (EMF) radiation exposure, such as:

  • recurring fatigue
  • nausea
  • disturbed sleep
  • frequent headaches
  • mental confusion**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

If pregnant or breast feeding, ask a doctor before using product.

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Store at room temperature.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Spray twice under the tongue three times per day for one month. For the next three months use same dosage one week per month.

Children 12 and under: Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (EMF) radiation exposure, such as:

  • recurring fatigue
  • nausea
  • disturbed sleep
  • frequent headaches
  • mental confusion**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY

LIDDELL LABORATORIES

201 APPLE BLVD.

WOODBINE, IA 51579

WWW.LIDDELL.NET

1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL

LABORATORIES


EST. 1994

DETOX

48 EMF

Electromagnetic

Radiation

May relieve symptoms of EMF
radiation: fatigue, headache,
disturbed sleep, confusion.


HOMEOPATHIC

DOCTOR FORMULATED

Readily absorbed. Safe.

No known side effects. Easy to use.

1.0 FL OZ (30 ml)

EMFEMF

EMFEMF

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0248-12024-07-01C16284748780-1ba0f9c33-110d-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0248-12024-01-30C16284748780-1ba0f9c33-110d-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0248-12022-04-19C16284748780-1ba0f9c33-110d-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0248-12021-01-29C16284748780-1ba0f9c33-110d-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50845-0248-1EMF30 mL in 1 BOTTLE, SPRAYSPRAY304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50845-0248EMF (ARGENTUM NITRICUM, ARNICA MONTANA, BAPTISIA TINCTORIA, CINCHONA OFFICINALIS, GALIUM APARINE, HEPAR SUIS, NATRUM CARBONICUM, PANAX GINSENG, PHOSPHORICUM ACIDUM, PHOSPHORUS, RHODODENDRON CHRYSANTHUM, STRONTIUM CARBONICUM, SULPHUR IODATUM, THUJA OCCIDENTALIS, X-RAY) SPRAY [LIDDELL LABORATORIES, INC.]4Current NDC, Legacy NDC, 1 package rows20240702_3fa1b8d3-7c09-431b-b843-03b2ef8a92b1.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-024850845-0248-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
EMFARGENTUM NITRICUM, ARNICA MONTANA, BAPTISIA TINCTORIA, CINCHONA OFFICINALIS, GALIUM APARINE, HEPAR SUIS, NATRUM CARBONICUM, PANAX GINSENG, PHOSPHORICUM ACIDUM, PHOSPHORUS, RHODODENDRON CHRYSANTHUM, STRONTIUM CARBONICUM, SULPHUR IODATUM, THUJA OCCIDENTALIS, X-RAYLiddell Laboratories, Inc.3fa1b8d3-7c09-431b-b843-03b2ef8a92b12024-07-01WarningsExact identifier
ndc (package): 50845-0248-1
ndc (product): 50845-0248
ndc11 (package): 50845024801
spl id: a12452f8-d7ea-4e84-b827-7483e69b5f48
spl set id: 3fa1b8d3-7c09-431b-b843-03b2ef8a92b1

Reported adverse events (FAERS/openFDA)#

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