Allerphenex

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2022-03-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:06:29

Label at a glance#

ProductAllerphenex II
Active ingredientACETYLCHOLINE CHLORIDE, ACETALDEHYDE, EPINEPHRINE, CAFFEIC ACID, CANDIDA ALBICANS, CHLOROGENIC ACID, CINNAMIC ACID, COUMARIN, CYSTEINE, GALLIC ACID MONOHYDRATE, PORK LIVER, HISTAMINE DIHYDROCHLORIDE, INDOLE, MALVIN, YEAST MANNAN, MENADIONE, NOREPINEPHRINE, OCTOPAMINE HYDROCHLORIDE, SUS SCROFA PANCREAS, PHENYL ISOTHIOCYANATE, PHLORIZIN, QUERCETIN, SALSOLINOL HYDROCHLORIDE, SEROTONIN HYDROCHLORIDE
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

(in each drop): 1.04% of Acetylcholine Chloride 200X, 400X, 800X, 1000X, Acetaldehyde 200X, 400X, 800X, 1000X, Adrenalinum 200X, 400X, 800X, 1000X, Caffeic Acid 200X, 400X, 800X, 1000X, Candida Albicans 12X, 30X, 60X, 100X, Chlorogenic Acid 200X, 400X, 800X, 1000X, Cinnamic Acid 200X, 400X, 800X, 1000X, Coumarinum 200X, 400X, 800X, 1000X, Cysteinum 200X, 400X, 800X, 1000X, Gallicum Acidum 200X, 400X, 800X, 1000X, Hepar Suis 200X, 400X, 800X, 1000X, Histaminum Hydrochloricum 200X, 400X, 800X, 1000X, Indolum 200X, 400X, 800X, 1000X, Malvin 200X, 400X, 800X, 1000X, Mannan 200X, 400X, 800X, 1000X, Menadione 200X, 400X, 800X, 1000X, Norepinephrine 200X, 400X, 800X, 1000X, Octopamine (Hydrochloride) 200X, 400X, 800X, 1000X, Pancreas Suis 200X, 400X, 800X, 1000X, Phenyl Isothiocyanate 200X, 400X, 800X, 1000X, Phloridzinum 200X, 400X, 800X, 1000X, Quercetin 200X, 400X, 800X, 1000X, Salsolinol 200X, 400X, 800X, 1000X, Serotonin (Hydrochloride) 200X, 400X, 800X, 1000X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with allergic reactions to phenolics.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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

May temporarily relieve symptoms associated with allergic reactions to phenolics.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Citric acid, Demineralized water, Potassium sorbate.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579   800.868.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

ALLERPHENEX II

1 fl. oz. (30 ml)

Allerphenex IIAllerphenex II

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0355-12022-03-10C16284748780-1ba0f9c33-4cee-a910-e053-dadaa90a0b85Drug Facts:
44911-0355-12021-01-29C16284748780-1ba0f9c33-4cee-a910-e053-dadaa90a0b85Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-035544911-0355-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
9f8d1f0d-2729-48d0-bdd1-57d137d2893f33c0a5ad-3a7a-44c3-862d-288f4a7bc5c42022-03-10WarningsExact identifier
spl id: 9f8d1f0d-2729-48d0-bdd1-57d137d2893f
spl set id: 33c0a5ad-3a7a-44c3-862d-288f4a7bc5c4

Reported adverse events (FAERS/openFDA)#

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