Histastat Pollen

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2023-05-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:31:20

Label at a glance#

ProductHistastat Pollen
Active ingredientBAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, ONION, AMBROSIA ARTEMISIIFOLIA WHOLE, ARSENIC TRIOXIDE, EUPHRASIA STRICTA, HISTAMINE DIHYDROCHLORIDE, SODIUM CHLORIDE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, SOLIDAGO VIRGAUREA FLOWERING TOP, SULFUR
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): 8.32% of Allium Cepa 12X, Ambrosia Artemisiaefolia 12X, Arsenicum Album 12X, Euphrasia Officinalis 12X, Histaminum Hydrochloricum 12X,Natrum Muriaticum 12X, Natrum Sulphuricum 12X, Nux Vomica 12X, Phosphorus 12X, Pulsatilla (Pratensis) 12X, Solidago Virgaurea 12X, Sulphur 12X; 0.10% of Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve sinus congestion due to hay fever and allergic rhinitis.**

**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 sinus congestion due to hay fever and allergic rhinitis.**

**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

HISTASTAT POLLEN

1 fl. oz. (30 ml)

Histastat PollenHistastat Pollen

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0577-12023-05-16C16284748780-1f386c649-bec9-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0577-12023-01-30C16284748780-1f386c649-bec9-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0577HISTASTAT POLLEN (BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM ALBUM, EUPHRASIA OFFICINALIS, HISTAMINUM HYDROCHLORICUM, NATRUM MURIATICUM, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), SOLIDAGO VIRGAUREA, SULPHUR) LIQUID [ENERGIQUE, INC.]2Legacy NDC20230517_3391ece7-8922-4afe-bbfc-de4640cefa11.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-057744911-0577-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
1f880e8f-1596-4c21-bb40-e5dad673ceb93391ece7-8922-4afe-bbfc-de4640cefa112023-05-16WarningsExact identifier
spl id: 1f880e8f-1596-4c21-bb40-e5dad673ceb9
spl set id: 3391ece7-8922-4afe-bbfc-de4640cefa11

Reported adverse events (FAERS/openFDA)#

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