Alcostat

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2025-03-04
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:40:51

Label at a glance#

ProductAlcostat
Active ingredientBETA VULGARIS WHOLE, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE FLOWER, CAPSICUM, CHELIDONIUM MAJUS WHOLE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, QUERCUS ROBUR NUT, SULFURIC ACID, ALCOHOL, 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): 11.08% of Capsicum Annuum 12X, Chelidonium Majus 12X, Ethylicum 12X, 30X, Lycopodium Clavatum 12X, Nux Vomica 12X, Quercus Glandium Spiritus 12X, Saccharum Officinale 30X, Sulphuricum Acidum 12X; 0.10% of Beta Vulgaris 3X, Taraxacum Officinale 3X, Trifolium Pratense 3X.

INDICATIONS:

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

Keep out of reach of children. 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

Demineralized water, 20% Ethanol.

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0182-12024-10-23C16284748780-1ba0f9c33-1db1-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0182-12024-01-30C16284748780-1ba0f9c33-1db1-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0182-12022-03-08C16284748780-1ba0f9c33-1db1-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0182-12021-01-29C16284748780-1ba0f9c33-1db1-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0182ALCOSTAT (BETA VULGARIS, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE, CAPSICUM ANNUUM, CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM, NOX VOMICA, QUERCUS GLANDIUM SPIRITUS, SULPHURICUM ACIDUM, ETHYLICUM, SACCHARUM OFFICINALE,) LIQUID [ENERGIQUE, INC.]6Legacy NDC20250306_f6d4fa65-8e3c-4640-84c8-a092c4a9a268.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M2
BETA VULGARISACTIVE INGREDIENT4G174V50512
CAPSICUMACTIVE INGREDIENT00UK7646FG2
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNN2
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4792
QUERCUS ROBUR NUTACTIVE INGREDIENTQ7MU1F4GLY2
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139192
SUCROSEACTIVE INGREDIENTC151H8M5542
SULFURIC ACIDACTIVE INGREDIENTO40UQP6WCF2
TARAXACUM OFFICINALEACTIVE INGREDIENT39981FM3752
TRIFOLIUM PRATENSE FLOWERACTIVE INGREDIENT4JS08388282
ALCOHOLACTIVE MOIETY3K9958V90M2
BETA VULGARISACTIVE MOIETY4G174V50512
CAPSICUMACTIVE MOIETY00UK7646FG2
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNN2
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4792
QUERCUS ROBUR NUTACTIVE MOIETYQ7MU1F4GLY2
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139192
SUCROSEACTIVE MOIETYC151H8M5542
SULFURIC ACIDACTIVE MOIETYO40UQP6WCF2
TARAXACUM OFFICINALEACTIVE MOIETY39981FM3752
TRIFOLIUM PRATENSE FLOWERACTIVE MOIETY4JS08388282
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-018244911-0182-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
e043596e-4175-4ea4-9902-b3fa7ab055d0f6d4fa65-8e3c-4640-84c8-a092c4a9a2682025-03-04WarningsExact identifier
spl id: e043596e-4175-4ea4-9902-b3fa7ab055d0
spl set id: f6d4fa65-8e3c-4640-84c8-a092c4a9a268

Reported adverse events (FAERS/openFDA)#

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