FDA.reportPublic FDA data

Light Root Compositum

Manufacturer
Uriel Pharmacy, Inc
Effective date
2026-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-11-03 06:04:51

Label at a glance#

ProductLight Root Compositum
Active ingredientCHINESE YAM, HELLEBORUS NIGER ROOT
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: 1-2 tablets. Ages 2-11: 1 tablet. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Each 200mg tablet contains:
66g Dioscorea batata (Light Root) Ø; Helleborus niger 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Glucose monohydrate, Magnesium stearate

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Memory and mood 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 by Uriel, East Troy, WI 53120
shopuriel.com Lot: Rev.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Light Root Compositum TabletsLight Root Compositum TabletsLig Root Com Tab

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-609648951-6096-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHINESE YAM29CIF30B1ZACTIB
HELLEBORUS NIGER ROOT608DGJ6815ACTIB
DEXTRATESG263MI44RUIACT
MAGNESIUM STEARATE70097M6I30IACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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