Apizastat

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2025-05-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:39:02

Label at a glance#

ProductApizastat
Active ingredientAVENA SATIVA FLOWERING TOP, BETA VULGARIS WHOLE, MEDICAGO SATIVA WHOLE, CHELIDONIUM MAJUS WHOLE, LARREA TRIDENTATA LEAF, PHYTOLACCA AMERICANA ROOT, URTICA DIOICA WHOLE, VERBASCUM THAPSUS WHOLE, VISCUM ALBUM FRUITING TOP, OXALIS ACETOSELLA LEAF, SILVER, CALCIUM FLUORIDE, THUJA OCCIDENTALIS LEAFY TWIG, THYMOL, BACILLUS ANTHRACIS IMMUNOSERUM RABBIT, BAPTISIA TINCTORIA ROOT, ALTERNANTHERA SESSILIS WHOLE, ALCOHOL, X-RAY EXPOSED (1000 RAD)
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): 6.24% of Alfalfa 2C, Anthracinum 12C, Argentum Metallicum 6C, Baptisia Tinctoria 12C, Calcarea Fluorica 6C, Chelidonium Majus 2C, Oxalis Acetosella 5C, Paloondo 2C, Paronichia Illecebrum 12C, Phytolacca Decandra 2C, Thuja Occidentalis 6C, Thymolum 7C, Urtica Dioica 2C, Verbascum Thapsus 2C, Viscum Album 2C, X-Ray 12C; 0.10% of Avena Sativa 1C, Beta Vulgaris 1C.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of fatigue, indigestion and abdominal pain with bloating.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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 symptoms of fatigue, indigestion and abdominal pain with bloating.**

**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

APIZASTAT

1 fl. oz. (30 ml)

ApizastatApizastat

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0551-12024-10-23C16284748780-1d6a99b39-c25b-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0551-12022-01-28C16284748780-1d6a99b39-c25b-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0551APIZASTAT (AVENA SATIVA, BETA VULGARIS, ALFALFA, CHELIDONIUM MAJUS, PALOONDO, PHYTOLACCA DECANDRA, URTICA DIOICA, VERBASCUM THAPSUS, VISCUM ALBUM, OXALIS ACETOSELLA, ARGENTUM METALLICUM, CALCAREA FLUORICA, THUJA OCCIDENTALIS, THYMOLUM, ANTHRACINUM, BAPTISIA TINCTORIA, PARONICHIA ILLECEBRUM, X-RAY) LIQUID [ENERGIQUE, INC.]3Legacy NDC20250519_e9ecdbfd-45a1-4741-9a14-0f7011ac5905.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-055144911-0551-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
3d6bd4a0-0eb2-4612-9272-655724d07632e9ecdbfd-45a1-4741-9a14-0f7011ac59052025-05-16WarningsExact identifier
spl id: 3d6bd4a0-0eb2-4612-9272-655724d07632
spl set id: e9ecdbfd-45a1-4741-9a14-0f7011ac5905

Reported adverse events (FAERS/openFDA)#

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