Nightshade Antigens

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2022-06-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:59:15

Label at a glance#

ProductNightshade Antigens
Active ingredientCAPSICUM, SOLANUM LYCOPERSICUM, EGGPLANT, SOLANUM TUBEROSUM, TOBACCO LEAF, ALUMINUM OXIDE, ARSENIC TRIOXIDE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, ANEMONE PULSATILLA
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): 3.44% of Alumina 12X, 15X, Arsenicum Album 12X, 15X, Capsicum Annuum 9X, 12X, 15X, 30X, Lycopersicum Esculentum 9X, 12X, 15X, 30X, Nux Vomica 12X, 15X, Phosphorus 12X, 15X, Pulsatilla (Pratensis) 12X, 15X, Solanum Melongena 12X, 15X, 30X, Solanum Tuberosum 9X, 12X, 15X, 30X, Tabacum 9X, 12X, 15X, 30X; 0.10% Solanum Melongena 9X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with nightshade 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 nightshade 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
NIGHTSHADE
ANTIGENS
1 fl. oz. (30 ml)

Nightshade AntigensNightshade Antigens

Nightshade AntigensNightshade Antigens

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0350-12022-06-15C16284748780-1d6a99b39-535e-a426-e053-dadaa90af4c2Drug Facts:
44911-0350-12022-01-28C16284748780-1d6a99b39-535e-a426-e053-dadaa90af4c2Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-035044911-0350-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
15670839-0ad5-4d6e-9f70-40f0f60ed6f5a4c85c11-f57f-44d5-8630-798f6e898df02022-06-01WarningsExact identifier
spl id: 15670839-0ad5-4d6e-9f70-40f0f60ed6f5
spl set id: a4c85c11-f57f-44d5-8630-798f6e898df0

Reported adverse events (FAERS/openFDA)#

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