Aller-Chord A

ALFALFA, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, BRYONIA (ALBA), CITRICUM ACIDUM, COUMARINUM, EUPHRASIA OFFICINALIS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, JUNIPERUS COMMUNIS, MUCOSA NASALIS SUIS, NATRUM SULPHURICUM, PHOSPHORUS, POTHOS FOETIDUS, PULSATILLA (VULGARIS), SOLIDAGO VIRGAUREA, SULPHUR, TANACETUM VULGARE, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE ORAL HUMAN OTC DRUG

Aller-Chord A is an FDA drug label for the active ingredient ALFALFA, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, BRYONIA (ALBA), CITRICUM ACIDUM, COUMARINUM, EUPHRASIA OFFICINALIS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, JUNIPERUS COMMUNIS, MUCOSA NASALIS SUIS, NATRUM SULPHURICUM, PHOSPHORUS, POTHOS FOETIDUS, PULSATILLA (VULGARIS), SOLIDAGO VIRGAUREA, SULPHUR, TANACETUM VULGARE, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE manufactured by Energetix Corporation 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 20260811.

Generic name: ALFALFA, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, BRYONIA (ALBA), CITRICUM ACIDUM, COUMARINUM, EUPHRASIA OFFICINALIS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, JUNIPERUS COMMUNIS, MUCOSA NASALIS SUIS, NATRUM SULPHURICUM, PHOSPHORUS, POTHOS FOETIDUS, PULSATILLA (VULGARIS), SOLIDAGO VIRGAUREA, SULPHUR, TANACETUM VULGARE, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE
Manufacturer: Energetix Corporation
Product type: HUMAN OTC DRUG
Route: ORAL
Dosage form: N/A
NDC: 64578-0057
Application: N/A
Label effective: 20260811

About this product

Aller-Chord A is an FDA-registered drug product whose active ingredient is ALFALFA, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, BRYONIA (ALBA), CITRICUM ACIDUM, COUMARINUM, EUPHRASIA OFFICINALIS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, JUNIPERUS COMMUNIS, MUCOSA NASALIS SUIS, NATRUM SULPHURICUM, PHOSPHORUS, POTHOS FOETIDUS, PULSATILLA (VULGARIS), SOLIDAGO VIRGAUREA, SULPHUR, TANACETUM VULGARE, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE. It is labelled by Energetix Corporation taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 64578-0057, label effective 20260811. 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 ALFALFA, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, BRYONIA (ALBA), CITRICUM ACIDUM, COUMARINUM, EUPHRASIA OFFICINALIS, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, JUNIPERUS COMMUNIS, MUCOSA NASALIS SUIS, NATRUM SULPHURICUM, PHOSPHORUS, POTHOS FOETIDUS, PULSATILLA (VULGARIS), SOLIDAGO VIRGAUREA, SULPHUR, TANACETUM VULGARE, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE are most often described in connection with: temporary relief, sneezing itching, congestion irritated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients 59.1 mL contains 2.27% of: Alfalfa 9X, 12X, 30X; Allium cepa 6X; Ambrosia 6X; Bryonia 6X, Citricum ac 12X; Coumarinum 12X, Euphrasia 6X; Glandula suprarenalis suis 9X, 12X; Hepar suis 9X, Histaminum hydrochloricum 12X, 30x, 12C, 30C; Hydrastis 9X, 12X, 30X; Juniperus com 9X, 12X, 30X; Mucosa nas 9X, 12X, 6C; Nat sulphuricum 12X; Phos 12X; Pothos 9X, 12X, 30X, Pulsatilla 12X; Solidago 9X, 12X, 30X, Sulphur 12X; Tanacetum 9X, 12X, 30X; Trifolium prat 9X, 12X, 30X. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Indications & Usage

Uses Temporary relief of sneezing, itching, congestion, irritated eyes.

Dosage & Administration

Take 30 drops orally twice daily or as directed by a healthcare professional. Consult a physician for use in children under 12 years of age or if symptoms worsen or persist.

Warnings

In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

Frequently asked questions

What is Aller-Chord A used for?
Uses Temporary relief of sneezing, itching, congestion, irritated eyes.

Who makes Aller-Chord A?
Energetix Corporation is the labeler of record for Aller-Chord A.

What form does Aller-Chord A 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 Aller-Chord A 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 Aller-Chord A 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.