Alcostat

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2025-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:32:16

Label at a glance#

ProductAlcostat
Active ingredientTARAXACUM OFFICINALE, AVENA SATIVA FLOWERING TOP, PASSIFLORA INCARNATA FLOWERING TOP, GOLD, CAPSICUM, CHELIDONIUM MAJUS WHOLE, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, QUERCUS ROBUR NUT, SULFURIC ACID, ALCOHOL, HUMAN BREAST TUMOR CELL, SUCROSE
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 7.14% Aurum Metallicum 12X, Avena Sativa 6X, Capsicum Annuum 12X, Carcinosin 30X, Chelidonium Majus 12X, Ethylicum 12X, 30X, Lachesis Mutus 12X, Lycopodium Clavatum 12X, Nox Vomica 12X, Passiflora Incarnata 6X, Quercus Glandium Spiritus 12X, Saccharum Officinale 30X, Sulphuricum Acidum 12X; 0.10% of Taraxacum Officinale 3X.

PURPOSE:

OTC - PURPOSE SECTION

May temporarily relieve loss of appetite, stomach upset, nausea, and craving of alcohol.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

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 broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve loss of appetite, stomach upset, nausea, and craving of alcohol.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Citric Acid, Demineralized Water, 0.12% Ethanol, Potassium Sorbate.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579

800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

ALCOSTAT

1 fl. oz. (30 ml)

ALCOSTATALCOSTAT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0735-1Alcostat30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0735ALCOSTAT (TARAXACUM OFFICINALE, AVENA SATIVA, PASSIFLORA INCARNATA, AURUM METALLICUM, CAPSICUM ANNUUM, CHELIDONIUM MAJUS, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NOX VOMICA, QUERCUS GLANDIUM SPIRITUS, SULPHURICUM ACIDUM, ETHYLICUM, CARCINOSIN, SACCHARUM OFFICINALE) LIQUID [ENERGIQUE, INC.]1Current NDC, 1 package rows20250306_77daea02-3c32-4ba3-a7a8-af79b13ddc06.zip

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
44911-073544911-0735-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

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
AlcostatTARAXACUM OFFICINALE, AVENA SATIVA, PASSIFLORA INCARNATA, AURUM METALLICUM, CAPSICUM ANNUUM, CHELIDONIUM MAJUS, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NOX VOMICA, QUERCUS GLANDIUM SPIRITUS, SULPHURICUM ACIDUM, ETHYLICUM, CARCINOSIN, SACCHARUM OFFICINALEEnergique, Inc.77daea02-3c32-4ba3-a7a8-af79b13ddc062025-02-27WarningsExact identifier
ndc (package): 44911-0735-1
ndc (product): 44911-0735
ndc11 (package): 44911073501
spl id: 737acb5d-f356-4cf4-87b0-3db55c91b5f3
spl set id: 77daea02-3c32-4ba3-a7a8-af79b13ddc06

Reported adverse events (FAERS/openFDA)#

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