FDA.reportPublic FDA data

Visiopar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-04-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:26:41

Label at a glance#

ProductVisiopar
Active ingredientEUPHRASIA STRICTA, SUS SCROFA EYE, GOLD, CALCIUM FLUORIDE, CAUSTICUM, CONIUM MACULATUM FLOWERING TOP, MAGNESIUM CARBONATE, PHOSPHORUS, SILICON DIOXIDE, PHYSOSTIGMA VENENOSUM SEED, OSMIUM, THUJA OCCIDENTALIS LEAFY TWIG
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): 8.33% of Aurum Metallicum 12X, Calcarea Fluorica 12X, Causticum 12X, Conium Maculatum 12X, Euphrasia Officinalis 6X, Eye (Suis) 8X, Magnesia Carbonica 12X, Osmium Metallicum 16X, Phosphorus 12X, Physostigma Venenosum 15X, Silicea 12X, Thuja Occidentalis 16X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve minor inflammation and pressure in the eyes and burning and swelling of the eyelids.**

**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 minor inflammation and pressure in the eyes and burning and swelling of the eyelids.**

**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

VISIOPAR

1 fl. oz. (30 ml)

VisioparVisiopar

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0559-12024-04-19C16284748780-11030e365-5125-111a-e063-dadaa90a10e2DRUG FACTS:
44911-0559-12024-01-30C16284748780-11030e365-5125-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0559-1Visiopar30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0559VISIOPAR (EUPHRASIA OFFICINALIS, EYE (SUIS), AURUM METALLICUM, CALCAREA FLUORICA, CAUSTICUM, CONIUM MACULATUM, MAGNESIA CARBONICA, PHOSPHORUS, SILICEA, PHYSOSTIGMA VENENOSUM, OSMIUM METALLICUM, THUJA OCCIDENTALIS) LIQUID [ENERGIQUE, INC.]3Current NDC, Legacy NDC, 1 package rows20240420_811f7626-0d21-49bd-8c31-9a5abec45c13.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
44911-055944911-0559-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
EUPHRASIA STRICTAC9642I91WLACTIB
SUS SCROFA EYEX3AOK514E6ACTIB
GOLD79Y1949PYOACTIB
CALCIUM FLUORIDEO3B55K4YKIACTIB
CAUSTICUMDD5FO1WKFUACTIB
CONIUM MACULATUM FLOWERING TOPQ28R5GF371ACTIB
MAGNESIUM CARBONATE0E53J927NAACTIB
PHOSPHORUS27YLU75U4WACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
PHYSOSTIGMA VENENOSUM SEEDCJV9E9IIOAACTIB
OSMIUM2E7M255OPYACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
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
VisioparEUPHRASIA OFFICINALIS, EYE (SUIS), AURUM METALLICUM, CALCAREA FLUORICA, CAUSTICUM, CONIUM MACULATUM, MAGNESIA CARBONICA, PHOSPHORUS, SILICEA, PHYSOSTIGMA VENENOSUM, OSMIUM METALLICUM, THUJA OCCIDENTALISEnergique, Inc.811f7626-0d21-49bd-8c31-9a5abec45c132024-04-19WarningsExact identifier
ndc (package): 44911-0559-1
ndc (product): 44911-0559
ndc11 (package): 44911055901
spl id: 1a403433-b407-46f7-b3a4-173af25de317
spl set id: 811f7626-0d21-49bd-8c31-9a5abec45c13

Reported adverse events (FAERS/openFDA)#

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