Lyme

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2020-04-09
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:36:38

Label at a glance#

ProductLyme HP
Active ingredientBAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA, GOLDENSEAL, BORRELIA BURGDORFERI, BABESIA MICROTI, EHRLICHIA CANIS, JAPANESE ENCEPHALITIS VIRUS, NEISSERIA MENINGITIDIS, HEPATITIS B VIRUS, ARSENIC TRIOXIDE, BRYONIA ALBA ROOT, CHELIDONIUM MAJUS, COLCHICUM AUTUMNALE BULB, KALMIA LATIFOLIA LEAF, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF
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

Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X, Hydrastis Canadensis 6X, Borrelia Burgdorferi Nosode 12X, 30X, 200X, Babesia Microti 20X, 200X, Ehrlichia Nosode (Canine) 20X, 200X,  Encephalitis Nosode 18X, 30X, 200X, Hepatitis B Nosode 30X, 200X, Meningococcus Nosode 15X, 30X, 200X, Arsenicum Album 30C, Bryonia (Alba) 30C, Chelidonium Majus 30X, Colchicum Autumnale 30C, Kalmia Latifolia 30C, Ledum Palustre 30C, Lycopodium Clavatum 30C, Phosphorus 30C, Rhus Tox 30C.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of aches and pains of joints and muscles as a consequence of Lyme Disease infection.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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

For temporary relief of aches and pains of joints and muscles as a consequence of Lyme Disease infection.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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

LYME HP

1 fl. oz. (30 ml)

Lyme HPLyme HP

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-043844911-0438-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
8afacabe-7fea-48ab-8104-79217aae54ad46ed6b7c-274a-46c4-aca0-1b7ca943e1b72020-04-09WarningsExact identifier
spl id: 8afacabe-7fea-48ab-8104-79217aae54ad
spl set id: 46ed6b7c-274a-46c4-aca0-1b7ca943e1b7

Reported adverse events (FAERS/openFDA)#

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