Lobelia comp. by Uriel Pharmacy, Inc. LOBELIA COMP. liquid

Lobelia comp. by

Drug Labeling and Warnings

Lobelia comp. by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION

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

ACTIVE INGREDIENT

Active Ingredients: Quercus Dec (Oak) 4X, Veronica Dec (Speedwell) 4X, Lobelia 6X, Plumbum met. (Lead) 12X

INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, 20% Organic cane alcohol
Prepared using rhythmical processes

PURPOSE

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

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.

QUESTIONS

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LOBELIA COMP. 
lobelia comp. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-6090
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J) (VERONICA OFFICINALIS FLOWERING TOP - UNII:9IH82J936J)	VERONICA OFFICINALIS FLOWERING TOP	4 [hp_X]  in 1 mL
QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W)	QUERCUS ROBUR WHOLE	4 [hp_X]  in 1 mL
LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P)	LEAD	12 [hp_X]  in 1 mL
LOBELIA SPICATA LEAF (UNII: 1G4GK01F67) (LOBELIA SPICATA LEAF - UNII:1G4GK01F67)	LOBELIA SPICATA LEAF	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-6090-3	60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy, Inc. (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy, Inc.		043471163	manufacture(48951-6090)