Pain and Fatigue Relief
Pain and Fatigue Relief is an FDA drug label for the active ingredient ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUM manufactured by The Magni Company administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230126.
- Generic name
- ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUM
- Manufacturer
- The Magni Company
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 43689-0015
- Application
- N/A
- Label effective
- 20230126
About this product
Pain and Fatigue Relief is an FDA-registered drug product whose active ingredient is ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUM. It is labelled by The Magni Company taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 43689-0015, label effective 20230126. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CONIINUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI BICHROMICUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, URICUM ACIDUM are most often described in connection with: indications temporarily, relieves widespread, aches pains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
INDICATIONS: Temporarily relieves widespread aches, pains, and stiffness with fatigue
Dosage & Administration
DIRECTIONS: • 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
Warnings
WARNINGS: • 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
Frequently asked questions
What is Pain and Fatigue Relief used for?
INDICATIONS: Temporarily relieves widespread aches, pains, and stiffness with fatigue
Who makes Pain and Fatigue Relief?
The Magni Company is the labeler of record for Pain and Fatigue Relief.
What form does Pain and Fatigue Relief come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Pain and Fatigue Relief prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Pain and Fatigue Relief been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.