FDA.reportPublic FDA data

AI Miasm

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-05-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:51

Label at a glance#

ProductAI Miasm
Active ingredientASTRAGALUS PROPINQUUS ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, HANDROANTHUS IMPETIGINOSUS BARK, SCROPHULARIA NODOSA WHOLE, THYROID, FORMIC ACID, PHOSPHORUS, SILICON DIOXIDE, SULFUR, THUJA OCCIDENTALIS LEAFY TWIG, GOLD
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): 14.23% of Aurum Metallicum 12X, Formicum Acidum 10X, Phosphorus 10X, Scrophularia Nodosa 8X, Sulphur 10X, Thuja Occidentalis 10X, Thyroidinum (Suis) 8X; 0.10% of Astragalus Membranaceus 3X, Echinacea (Angustifolia) 3X, Silicea 10X, Tabebuia Impetiginosa 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of rash, itching, swelling, redness, and minor joint pain.**

**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 symptoms of rash, itching, swelling, redness, and minor joint pain.**

**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
AI MIASM
1 fl. oz. (30 ml)

AI MIASMAI MIASM

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0628-12024-05-02C16284748780-1f386c649-b46b-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0628-12023-01-30C16284748780-1f386c649-b46b-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0628-1AI Miasm30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0628AI MIASM (ASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), TABEBUIA IMPETIGINOSA, SCROPHULARIA NODOSA, THYROIDINUM (SUIS), FORMICUM ACIDUM, PHOSPHORUS, SILICEA, SULPHUR, THUJA OCCIDENTALIS, AURUM METALLICUM) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20240504_df829e4a-c982-4d02-b318-38b1fbc5072d.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-062844911-0628-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ASTRAGALUS PROPINQUUS ROOT922OP8YUPFACTIB
ECHINACEA ANGUSTIFOLIA WHOLEVB06AV5US8ACTIB
HANDROANTHUS IMPETIGINOSUS BARK6GLA1946WXACTIB
SCROPHULARIA NODOSA WHOLE7H443NUB2TACTIB
THYROID6RV024OAUQACTIB
FORMIC ACID0YIW783RG1ACTIB
PHOSPHORUS27YLU75U4WACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
SULFUR70FD1KFU70ACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
GOLD79Y1949PYOACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
AI MiasmASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), TABEBUIA IMPETIGINOSA, SCROPHULARIA NODOSA, THYROIDINUM (SUIS), FORMICUM ACIDUM, PHOSPHORUS, SILICEA, SULPHUR, THUJA OCCIDENTALIS, AURUM METALLICUMEnergique, Inc.df829e4a-c982-4d02-b318-38b1fbc5072d2024-05-02WarningsExact identifier
ndc (package): 44911-0628-1
ndc (product): 44911-0628
ndc11 (package): 44911062801
spl id: 5dd7ee51-2958-478e-aca3-c96af93f1c0d
spl set id: df829e4a-c982-4d02-b318-38b1fbc5072d

Reported adverse events (FAERS/openFDA)#

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