Grain and Seed Antigens

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2021-06-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:44:03

Label at a glance#

ProductGrain and Seed Antigens
Active ingredientBAMBUSA VULGARIS TOP, BARLEY, CORN, COTTON SEED, FLAX SEED, MILLET, OAT, POPPY SEED, BROWN RICE, RYE, SAFFLOWER, SESAME SEED, SORGHUM, SOYBEAN, SUGARCANE, HELIANTHUS ANNUUS FLOWERING TOP, WHEAT, ARSENIC TRIOXIDE, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, 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): 11.11% of Arsenicum Album 12X, 15X, Lycopodium Clavatum 12X, 15X, Natrum Muriaticum 12X, 15X, Sulphur 12X, 15X; 2.78% of Bamboo 12X, 15X, 18X, 33X, Barley 12X, 15X, 18X, 33X, Corn 12X, 15X, 18X, 33X, Cotton Seed 12X, 15X, 18X, 33X, Flax Seed (Linum Usitatissimum) 12X, 15X, 18X, 33X, Millet 12X, 15X, 18X, 33X, Milo 12X, 15X, 18X, 33X, Oat 12X, 15X, 18X, 33X, Poppy Seed 12X, 15X, 18X, 33X, Rice 12X, 15X, 18X, 33X, Rye 12X, 15X, 18X, 33X, Safflower 12X, 15X, 18X, 33X, Sesame 12X, 15X, 18X, 33X, Sorghum 12X, 15X, 18X, 33X, Soy Bean 12X, 15X, 18X, 33X, Sugarcane 12X, 15X, 18X, 33X, Sunflower (Helianthus Annuus) 12X, 15X, 18X, 33X, Wheat 12X, 15X, 18X, 33X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with grains and seed allergies such as runny nose and sneezing.**

**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 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 symptoms associated with grains and seed allergies such as runny nose and sneezing.**

**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     800.868.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

GRAIN AND SEED  

ANTIGENS

1 fl. oz. (30 ml)

Grain and Seed AntigensGrain and Seed Antigens

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0417-12021-06-02C16284748780-1ba0f9c33-3a5f-a910-e053-dadaa90a0b85Drug Facts:
44911-0417-12021-01-29C16284748780-1ba0f9c33-3a5f-a910-e053-dadaa90a0b85Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-041744911-0417-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
742f40ae-c48e-4b1c-a41b-4b1ea787428c4be0c1b3-f854-441b-854e-4c7c929b3fda2021-06-01WarningsExact identifier
spl id: 742f40ae-c48e-4b1c-a41b-4b1ea787428c
spl set id: 4be0c1b3-f854-441b-854e-4c7c929b3fda

Reported adverse events (FAERS/openFDA)#

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