FDA.reportPublic FDA data

Reynoutria Lyme

Manufacturer
Uriel Pharmacy Inc.
Effective date
2021-03-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:45:21

Label at a glance#

ProductReynoutria Lyme
Active ingredientAPIS MELLIFERA, HELLEBORUS NIGER ROOT, ASTRAGALUS PROPINQUUS ROOT, SILICON DIOXIDE, GOLD, DIPSACUS FULLONUM WHOLE, REYNOUTRIA JAPONICA LEAF, SILVER, COPPER, ASTRAGALUS CHINENSIS SEED
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Reynoutria japonica (Japanese knotweed) 3X, Dipsacus sylvestris (Teasel) 4X, Helleborus (Christmas rose) 4X, Astragalus membraceus e rad. (Milk vetch) 6X, Argentum (Silver) 17X, Cuprum (Copper) 17X, Quartz (Rock crystal) 17X, Apis (Honeybee) 21X, Astragalus membraceus e fol. et sem. (Milk vetch) 30X, Aurum (Metallic gold) 30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 20% Organic cane alcohol

OTC - PURPOSE SECTION

Use: Immune support.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com Lot#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Reynoutria Lyme LiquidReynoutria Lyme Liquid

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-837248951-8372-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
APIS MELLIFERA7S82P3R43ZACTIB
HELLEBORUS NIGER ROOT608DGJ6815ACTIB
ASTRAGALUS PROPINQUUS ROOT922OP8YUPFACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
WATER059QF0KO0RIACT
GOLD79Y1949PYOACTIB
ALCOHOL3K9958V90MIACT
DIPSACUS FULLONUM WHOLE1FT87R544SACTIB
REYNOUTRIA JAPONICA LEAF2540B7G25GACTIB
SILVER3M4G523W1GACTIB
COPPER789U1901C5ACTIB
ASTRAGALUS CHINENSIS SEEDU046B39ADEACTIB

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
eac54fa4-9611-4aef-e053-2a95a90ab99fbd5d5a7d-6b96-ca38-e053-2a95a90a6a762022-10-11WarningsExact identifier
spl set id: bd5d5a7d-6b96-ca38-e053-2a95a90a6a76

Reported adverse events (FAERS/openFDA)#

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