Chicory Ginger Bitters

Manufacturer
Uriel Pharmacy Inc | Uriel Pharmacy Inc.
Effective date
2022-05-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:00:44

Label at a glance#

ProductChicory Ginger Bitters
Active ingredientACORUS CALAMUS ROOT, TURMERIC, GENTIANA LUTEA ROOT, SILYBUM MARIANUM SEED, CHICORY ROOT, GINGER, CHELIDONIUM MAJUS, BLACK PEPPER, WORMWOOD
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily before or after meals and/or snacks. Ages 12 and older: 1/4 teaspoon. Ages 2-11: 1/8 teaspoon. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:Milk thistle seed extract, Gentian root extract, Chicory root extract,Wormwood extract, Ginger root extract, Sweet flag root extract, Greater celandine root extract,Turmeric root extract, Black pepper corns extract

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Lime flavor

OTC - PURPOSE SECTION

Uses: Improves digestion; eases gas and indigestion.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Warnings: 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.

SHAKE WELL BEFORE USE. REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 90 DAYS OF OPENING.

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

Chicory GingerChicory Ginger

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-324048951-3240-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
26cd90b1-d262-d901-e063-6394a90a9b68c46ab81e-e1f1-0c3e-e053-2a95a90a0db92024-11-13WarningsExact identifier
spl set id: c46ab81e-e1f1-0c3e-e053-2a95a90a0db9

Reported adverse events (FAERS/openFDA)#

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