Hypothalmupar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2019-01-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:34:03

Label at a glance#

ProductHypothalmupar
Active ingredientAMERICAN GINSENG, GINKGO, CENTELLA ASIATICA, SUS SCROFA CEREBRUM, SUS SCROFA PITUITARY GLAND, SUS SCROFA HYPOTHALAMUS, PHOSPHORUS, SILICON DIOXIDE
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, 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

Aralia Quinquefolia 3X, Ginkgo Biloba 3X, Hydrocotyle Asiatica 3X, Cerebrum Suis 6X, Hypophysis Suis 6X, Hypothalamus (Bovine) 12X, Phosphorus 12X, Silicea 12X.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of weakness, exhaustion and vertigo, and difficult mental concentration.**


**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of weakness, exhaustion and vertigo, and difficult mental concentration.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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

HYPOTHALMUPAR

1 fl. oz. (30 ml)

HypothalmuparHypothalmupar

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-042144911-0421-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
b3f1ed5a-3a49-47b2-be0f-af5d5c05fa1ce0a4e3c3-5ec0-4ad7-ae0d-72a14040f12f2019-01-03WarningsExact identifier
spl id: b3f1ed5a-3a49-47b2-be0f-af5d5c05fa1c
spl set id: e0a4e3c3-5ec0-4ad7-ae0d-72a14040f12f

Reported adverse events (FAERS/openFDA)#

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