FDA.reportPublic FDA data

Pain and Fatigue Relief

Manufacturer
The Magni Company | Apotheca Company
Effective date
2023-01-26
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:19:58

Label at a glance#

ProductPain and Fatigue Relief
Active ingredientACONITUM NAPELLUS WHOLE, ARSENIC TRIOXIDE, ATROPA BELLADONNA, CONIINE, GELSEMIUM SEMPERVIRENS ROOT, HYPERICUM PERFORATUM WHOLE, POTASSIUM DICHROMATE, LACTIC ACID, DL-, PHOSPHORIC ACID, TOXICODENDRON PUBESCENS LEAF, URIC ACID
Label structure10 sections

Dosage and administration

• Adults and children 12 years and above: Dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician • Children under 12: Consult a physician • Take at least 10 minutes before or after eating or drinking

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Aconitum Napellus 30C, Arsenicum Album 30C, Belladonna 30C, Coniinum 30C, Gelsemium Sempervirens 30C, Hypericum Perforatum 3X, 30C, Kali Bichromicum 30C, Lacticum Acidum 30C, Phosphoricum Acidum 30C, Rhus Tox 30C, Uricum Acidum 30C

INDICATIONS:

OTC - PURPOSE SECTION

Temporarily relieves widespread aches, pains, and stiffness with fatigue

WARNINGS:

WARNINGS SECTION

• If pregnant or breastfeeding, ask a health professional before use

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

• If symptoms persist for more than 7 days or worsen, consult your physician

OTHER INFORMATION:

OTHER SAFETY INFORMATION

• Store tightly closed in a cool, dry place.

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

• The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United

   States

• These statements are supported by the traditional homeopathic principles

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

• Adults and children 12 years and above: Dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician

• Children under 12: Consult a physician

• Take at least 10 minutes before or after eating or drinking

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate, Microcrystalline Cellulose

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 contact a Poison Control Center right away

INDICATIONS:

INDICATIONS & USAGE SECTION

Temporarily relieves widespread aches, pains, and stiffness with fatigue

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by: The Magni Group, Inc.   McKinney, TX 75071 USA

www.magilife.com                                   1-800-645-9199

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAGNILIFE
PAIN & FATIGUE
RELIEF

For Widespread Aches, Pains
& Stiffness with Fatigue

√ Muscle Aches
√ Arthritis
√ Joint Pain
√ Stiffness
√ Fatigue

125 Tablets

Pain & Fatigue Relief LBLPain & Fatigue Relief LBL

Pain & Fatigue Relief CTNPain & Fatigue Relief CTN

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43689-0015-22022-01-10C16284748780-1ba0f9c33-3cf9-a910-e053-dadaa90a0b85DRUG FACTS:
43689-0015-22021-01-29C16284748780-1ba0f9c33-3cf9-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43689-0015-1Pain and Fatigue Relief125 in 1 BOTTLETABLET1255
43689-0015-2Pain and Fatigue Relief1 in 1 CARTONTABLET15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43689-0015PAIN AND FATIGUE RELIEF (ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUM) TABLET [THE MAGNI COMPANY]5Current NDC, Legacy NDC, 2 package rows20230127_7c689153-2002-421d-b573-76b0052550e0.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JD1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
CONIINEACTIVE INGREDIENTC479P32L2D1
GELSEMIUM SEMPERVIRENS ROOTACTIVE INGREDIENT639KR60Q1Q1
HYPERICUM PERFORATUMACTIVE INGREDIENTXK4IUX8MNB1
LACTIC ACID, DL-ACTIVE INGREDIENT3B8D35Y7S41
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
POTASSIUM DICHROMATEACTIVE INGREDIENTT4423S18FM1
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A1
URIC ACIDACTIVE INGREDIENT268B43MJ251
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JD1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
CONIINEACTIVE MOIETYC479P32L2D1
DICHROMATE IONACTIVE MOIETY9LKY4BFN2V1
GELSEMIUM SEMPERVIRENS ROOTACTIVE MOIETY639KR60Q1Q1
HYPERICUM PERFORATUMACTIVE MOIETYXK4IUX8MNB1
LACTIC ACID, DL-ACTIVE MOIETY3B8D35Y7S41
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A1
URIC ACIDACTIVE MOIETY268B43MJ251
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43689-001543689-0015-1, 43689-0015-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUS WHOLEU0NQ8555JDACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
CONIINEC479P32L2DACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
HYPERICUM PERFORATUM WHOLEXK4IUX8MNBACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
LACTIC ACID, DL-3B8D35Y7S4ACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
URIC ACID268B43MJ25ACTIB
LACTOSEJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates

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
Pain and Fatigue ReliefACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUMThe Magni Company7c689153-2002-421d-b573-76b0052550e02023-01-26WarningsExact identifier
ndc (package): 43689-0015-2
ndc (package): 43689-0015-1
ndc (product): 43689-0015
ndc11 (package): 43689001501
ndc11 (package): 43689001502
spl id: ec83ed89-ee4e-408e-8dcf-244a762a5e9b
spl set id: 7c689153-2002-421d-b573-76b0052550e0

Reported adverse events (FAERS/openFDA)#

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