Infectistat

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2022-03-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:04:52

Label at a glance#

ProductInfectistat
Active ingredientBAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA, LOBELIA INFLATA, LOMATIUM DISSECTUM ROOT, GOLDENSEAL, SUS SCROFA LUNG, PHYTOLACCA AMERICANA ROOT, COMFREY ROOT, ACONITUM NAPELLUS, ARSENIC TRIOXIDE, ATROPA BELLADONNA, BRYONIA ALBA ROOT, CAUSTICUM, EUPATORIUM PERFOLIATUM FLOWERING TOP, FERROSOFERRIC PHOSPHATE, GELSEMIUM SEMPERVIRENS ROOT, HYPERICUM PERFORATUM, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, SODIUM SULFATE, PHOSPHORUS, ANEMONE PRATENSIS, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, SULFUR, RANCID BEEF
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 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age. WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 4.53% of Hydrastis Canadensis 6X, Lung (Suis) 6X, Phytolacca Decandra 6X, Symphytum Officinale 6X; Aconitum Napellus 12X, Arsenicum Album 12X, Belladonna 12X, Bryonia 12X, Causticum 12X, Eupatorium Perfoliatum 12X, Ferrum Phosphoricum 12X, Gelsemium Sempervirens 12X, Hypericum Perforatum 12X, Kali Carbonicum 12X, Lachesis Mutus 12X, Natrum Sulphuricum 12X, Phosphorus 12X, Pulsatilla (Pratensis) 12X, Rhus Tox 12X, Silicea 12X, Sulphur 12X; Pyrogenium 30X. 0.10% of Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X, Lobelia Inflata 3X, Lomatium Dissectum 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.**

**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 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.**

**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

INFECTISTAT

1 fl. oz. (30 ml)

InfectistatInfectistat

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0510-12022-03-28C16284748780-1d6a99b39-7c73-a426-e053-dadaa90af4c2Drug Facts:
44911-0510-12022-01-28C16284748780-1d6a99b39-7c73-a426-e053-dadaa90af4c2Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-051044911-0510-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
51e182c6-26b2-45a4-b59e-0f72551996f234f82c3a-d22b-4903-992a-e10726c7fce92022-03-28WarningsExact identifier
spl id: 51e182c6-26b2-45a4-b59e-0f72551996f2
spl set id: 34f82c3a-d22b-4903-992a-e10726c7fce9

Reported adverse events (FAERS/openFDA)#

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