CMV Stat

Manufacturer
Energique, Inc | Apotheca Company
Effective date
2022-03-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:06:33

Label at a glance#

ProductCMV Stat
Active ingredientECHINACEA ANGUSTIFOLIA, LOMATIUM DISSECTUM ROOT, TABEBUIA IMPETIGINOSA BARK, GOLDENSEAL, PHYTOLACCA AMERICANA ROOT, ARANEUS DIADEMATUS, IPECAC, IRIDIUM, LACHESIS MUTA VENOM, HYDROCHLORIC ACID, TOXICODENDRON PUBESCENS LEAF, HUMAN HERPESVIRUS 5
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 3 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): 9.06% of Aranea Diadema 12X, Cytomegalovirus Nosode 30X, 60X, 200X, Hydrastis Canadensis 6X, Ipecacuanha 12X, Iridium Metallicum 12X, Lachesis Mutus 12X, Muriaticum Acidum 12X, Phytolacca Decandra 6X, Rhus Tox 12X; 0.10% of Echinacea (Angustifolia) 3X, Lomatium Dissectum 3X, Tabebuia Impetiginosa 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve fever with digestive symptoms and muscular aches and pains.**

**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 3 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 fever with digestive symptoms and muscular aches and pains.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

SPL UNCLASSIFIED 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
CMV STAT
1 fl. oz. (30 ml)

CMV StatCMV Stat

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0517-12022-03-10C16284748780-1ba0f9c33-2018-a910-e053-dadaa90a0b85Drug Facts:
44911-0517-12021-01-29C16284748780-1ba0f9c33-2018-a910-e053-dadaa90a0b85Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-051744911-0517-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
fa57f2f9-2353-48ab-ad5a-c51b9675632ea0a71248-037b-4ab5-8bc3-ee28054969de2022-03-10WarningsExact identifier
spl id: fa57f2f9-2353-48ab-ad5a-c51b9675632e
spl set id: a0a71248-037b-4ab5-8bc3-ee28054969de

Reported adverse events (FAERS/openFDA)#

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