Bach Original Flower Remedies Agrimony

AGRIMONIA EUPATORIA ORAL HUMAN OTC DRUG

Bach Original Flower Remedies Agrimony is an FDA drug label for the active ingredient AGRIMONIA EUPATORIA manufactured by Nelsons Bach USA Limited 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 20220926.

Generic name
AGRIMONIA EUPATORIA
Manufacturer
Nelsons Bach USA Limited
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
57687-200
Application
N/A
Label effective
20220926

About this product

Bach Original Flower Remedies Agrimony is an FDA-registered drug product whose active ingredient is AGRIMONIA EUPATORIA. It is labelled by Nelsons Bach USA Limited taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 57687-200, label effective 20220926. It is one of 2 FDA drug label records sharing the active ingredient AGRIMONIA EUPATORIA. 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 AGRIMONIA EUPATORIA are most often described in connection with: relief naturally, occurring simple, nervous tension. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Agrimony (Agrimonia eupatoria) 5X HPUS ‘HPUS’ indicates the ingredient is in the official Homeopathic Pharmacopoeia of the United States

Indications & Usage

Use For relief of naturally occurring simple nervous tension

Dosage & Administration

Directions Take 2 drops directly on the tongue or add to a beverage & sip. Repeat as needed throughout the day. Children under 2: ask a doctor before use.

Warnings

Warnings Consult a doctor if symptoms last for more than 7 days or worsen Keep out of reach of children. If pregnant or breast-feeding , ask a health professional before use.

More products with the same ingredient

AGRIMONIA EUPATORIA

Bach Original Flower Remedies

Nelson Bach USA Limited View label

How products containing AGRIMONIA EUPATORIA compare

FDA lists 2 drug label records with AGRIMONIA EUPATORIA as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Nelson Bach USA Limited 1
— — Nelsons Bach USA Limited 1
— — — —
— — — —
— — — —

Frequently asked questions

What is Bach Original Flower Remedies Agrimony used for?
Use For relief of naturally occurring simple nervous tension

Who makes Bach Original Flower Remedies Agrimony?
Nelsons Bach USA Limited is the labeler of record for Bach Original Flower Remedies Agrimony. 2 FDA label records share the active ingredient AGRIMONIA EUPATORIA, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Bach Original Flower Remedies Agrimony 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 Bach Original Flower Remedies Agrimony 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.

Are there other products containing AGRIMONIA EUPATORIA?
Yes. 2 FDA drug label records list AGRIMONIA EUPATORIA as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Bach Original Flower Remedies Agrimony 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.