Anxiety Relief

ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, AURUM METALLICUM, GELSEMIUM SEMPERVIRENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI CARBONICUM, MOSCHUS, NATRUM MURIATICUM, PIPER METHYSTICUM ORAL HUMAN OTC DRUG

Anxiety Relief is an FDA drug label for the active ingredient ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, AURUM METALLICUM, GELSEMIUM SEMPERVIRENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI CARBONICUM, MOSCHUS, NATRUM MURIATICUM, PIPER METHYSTICUM manufactured by NaturalCare 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 20260415.

Generic name
ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, AURUM METALLICUM, GELSEMIUM SEMPERVIRENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI CARBONICUM, MOSCHUS, NATRUM MURIATICUM, PIPER METHYSTICUM
Manufacturer
NaturalCare
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
70163-0047
Application
N/A
Label effective
20260415

About this product

Anxiety Relief is an FDA-registered drug product whose active ingredient is ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, AURUM METALLICUM, GELSEMIUM SEMPERVIRENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI CARBONICUM, MOSCHUS, NATRUM MURIATICUM, PIPER METHYSTICUM. It is labelled by NaturalCare taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 70163-0047, label effective 20260415. 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, ARGENTUM NITRICUM, ARSENICUM ALBUM, AURUM METALLICUM, GELSEMIUM SEMPERVIRENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI CARBONICUM, MOSCHUS, NATRUM MURIATICUM, PIPER METHYSTICUM are most often described in connection with: help temporarily, relieve occasional, minor anxiety, fear anguish, worry everyday, life nervousness, claims based, traditional homeopathic. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENT: (in each tablet) Aconitum Napellus 9X 0.0005%, Argentum Nitricum 8X 0.0005%, Arsenicum Album 9X 0.0005%, Aurum Metallicum 8X 0.0005%, Gelsemium Sempervirens 8X, 30X 0.0005%, Hyoscyamus Niger 6X, 12X 0.0005%, Ignatia Amara 6X, 12X 0.0005%, Kali Carbonicum 12X, 30X 0.0005%, Moschus 12X, Natrum Muriaticum 6X, 12X, 30X 0.0005%, Piper Methysticum 7X, 9X, 12X, 30X 0.0005%.

Indications & Usage

USES: May help temporarily relieve ■ occasional minor anxiety ■ fear ■ anguish ■ stress and worry of everyday life ■ nervousness* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: Adults and children over the age of 12: ■ dissolve 1-2 tablets under the tongue 3 times daily.

Warnings

WARNINGS: Stop use and ask a doctor if ■ symptoms persist for more than 30 days ■ symptoms become more severe If pregnant or breast-feeding, 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. Do not use if tamper evident seal is missing or open. ■ Store at room temperature (65-80ºF)

Frequently asked questions

What is Anxiety Relief used for?
USES: May help temporarily relieve ■ occasional minor anxiety ■ fear ■ anguish ■ stress and worry of everyday life ■ nervousness* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Who makes Anxiety Relief?
NaturalCare is the labeler of record for Anxiety Relief.

What form does Anxiety 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 Anxiety 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 Anxiety 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.