FDA.reportPublic FDA data

Vegetable Antigens

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2022-06-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:57:46

Label at a glance#

ProductVegetable Antigens
Active ingredientONION, GARLIC, CELERY SEED, BEET, CAULIFLOWER, CABBAGE, BROCCOLI, KALE, TURNIP, CHICKPEA, CUCUMBER, SOYBEAN, LETTUCE, LENTIL, PARSNIP, KIDNEY BEAN, LIMA BEAN, STRING BEAN, RADISH, SPINACH, ARSENIC TRIOXIDE, BRYONIA ALBA ROOT, HELLEBORUS NIGER ROOT, LYCOPODIUM CLAVATUM SPORE, KEROSENE
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) : 9.09% of Arsenicum Album 12X, 15X, Bryonia (Alba) 12X, 15X, Helleborus Niger 12X, 15X, Lycopodium Clavatum 12X, 15X, Petroleum 12X, 15X; 2.27% of Allium Cepa 12X, 15X, 18X, 30X, Allium Sativum 12X, 15X, 18X, 30X, Apium Graveolens 12X, 15X, 18X, 30X, Beta Vulgaris 12X, 15X, 18X, 30X, Brassica Oleracea Var. Botrytis 12X, 15X, 18X, 30X, Brassica Oleracea Var. Capitata 12X, 15X, 18X, 30X, Brassica Oleracea Var. Italica 12X, 15X, 18X, 30X, Brassica Oleracea Var. Sabellica 12X, 15X, 18X, 30X, Brassica Rapa Var. Rapa 12X, 15X, 18X, 30X, Cicer Arietinum 12X, 15X, 18X, 30X, Cucumis Sativus 12X, 15X, 18X, 30X, Glycine Max 12X, 15X, 18X, 30X, Lactuca Sativa 12X, 15X, 18X, 30X, Lens Culinaris 12X, 15X, 18X, 30X, Pastinaca Sativa 12X, 15X, 18X, 30X, Phaseolus 12X, 15X, 18X, 30X, Phaseolus Lunatus 12X, 15X, 18X, 30X, Phaseolus Vulgaris 12X, 15X, 18X, 30X, Raphanus Sativus 12X, 15X, 18X, 30X, Spinacia Oleracea 12X, 15X, 18X, 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with vegetable allergies.**

**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 vegetable allergies.**

**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

VEGETABLE

ANTIGENS

1 fl. oz. (30 ml)

Vegetable AntigensVegetable Antigens

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0361-12022-06-30C16284748780-1d6a99b39-383b-a426-e053-dadaa90af4c2Drug Facts:
44911-0361-12022-01-28C16284748780-1d6a99b39-383b-a426-e053-dadaa90af4c2Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-036144911-0361-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
ONION492225Q21HACTIB
GARLICV1V998DC17ACTIB
CELERY SEED1G1EAA320LACTIB
BEETN487KM8COKACTIB
CAULIFLOWER138LUT2DWVACTIB
CABBAGEGW0W1Y9I97ACTIB
BROCCOLIUOI4FT57BZACTIB
KALE0Y3L4J38H1ACTIB
TURNIPZ38C7FBM49ACTIB
CHICKPEAN91637DNW9ACTIB
CUCUMBERYY7C30VXJTACTIB
SOYBEANL7HT8F1ZODACTIB
LETTUCE5PO6NN3RRJACTIB
LENTIL6O38V6B52OACTIB
PARSNIPL2V28YP49SACTIB
KIDNEY BEANM98C8416QOACTIB
LIMA BEAN112YH1ZMX2ACTIB
STRING BEANN9D69B2Q7YACTIB
RADISHEM5RP35463ACTIB
SPINACH6WO75C6WVBACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
HELLEBORUS NIGER ROOT608DGJ6815ACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
KEROSENE1C89KKC04EACTIB
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
87dde3a8-7137-46bf-9b1d-87661eee9320b22e4ad5-1244-4d4a-9616-1c591d0e93f22022-06-30WarningsExact identifier
spl id: 87dde3a8-7137-46bf-9b1d-87661eee9320
spl set id: b22e4ad5-1244-4d4a-9616-1c591d0e93f2

Reported adverse events (FAERS/openFDA)#

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