FDA.reportPublic FDA data

Reynoutria Lyme

Manufacturer
Uriel Pharmacy, Inc. | Uriel Pharmacy, Inc
Effective date
2022-10-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:18:17

Label at a glance#

ProductReynoutria Lyme
Active ingredientCOPPER, SILICON DIOXIDE, APIS MELLIFERA, ASTRAGALUS CHINENSIS SEED, GOLD, SILVER, HELLEBORUS NIGER ROOT, DIPSACUS FULLONUM WHOLE, ASTRAGALUS PROPINQUUS ROOT, REYNOUTRIA JAPONICA LEAF
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 membranaceus 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
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Reynoutria Lyme LiquidReynoutria Lyme Liquid

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8396-3Reynoutria Lyme60 mL in 1 BOTTLE, GLASSLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8396REYNOUTRIA LYME LIQUID [URIEL PHARMACY, INC.]1Legacy NDC, 1 package rows20221012_eac885e5-e8fd-a7c9-e053-2995a90a566a.zip

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
48951-839648951-8396-3

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
COPPER789U1901C5ACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
APIS MELLIFERA7S82P3R43ZACTIB
ASTRAGALUS CHINENSIS SEEDU046B39ADEACTIB
GOLD79Y1949PYOACTIB
SILVER3M4G523W1GACTIB
WATER059QF0KO0RIACT
HELLEBORUS NIGER ROOT608DGJ6815ACTIB
DIPSACUS FULLONUM WHOLE1FT87R544SACTIB
ASTRAGALUS PROPINQUUS ROOT922OP8YUPFACTIB
ALCOHOL3K9958V90MIACT
REYNOUTRIA JAPONICA LEAF2540B7G25GACTIB

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
eac885e5-e8fe-a7c9-e053-2995a90a566aeac885e5-e8fd-a7c9-e053-2995a90a566a2022-10-11WarningsExact identifier
spl id: eac885e5-e8fe-a7c9-e053-2995a90a566a
spl set id: eac885e5-e8fd-a7c9-e053-2995a90a566a

Reported adverse events (FAERS/openFDA)#

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