DIURETIC- apis mellifica, berberis vulgaris, helleborus niger, juniperus communis, prunus spinosa, strophanthus hispidus, taraxacum officinale, uva-ursi spray
Liddell Laboratories, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Drug Facts

ACTIVE INGREDIENTS:

Apis Mellifica 3X, Berberis Vulgaris 3X, Helleborus Niger 3X, Juniperus Communis 1X, Prunus Spinosa 3X, Strophanthus Hispidus 6X, Taraxacum Officinale 1X, Uva-Ursi 3X

INDICATIONS:

May temporarily relieve symptoms associated with fluid accumulation: puffiness, distended bladdder, suppressed urination.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

If symptoms persist, consult a doctor.

If pregnant or breast feeding, ask a doctor before use.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

DIRECTIONS:

Adults and children over 12: Spray twice under the tongue 3 times per day.

Children 12 and under: Consult a doctor prior to use.

INACTIVE INGREDIENTS:

Organic alcohol 20% v/v, Purrified water.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

INDICATIONS:

May temporarily relieve symptoms associated with fluid accumulation: puffiness, distended bladdder, suppressed urination.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

QUESTIONS:

DIST. BY LIDDELL LABORATORIES INC.

WOODBINE, IA 51579

WWW.LIDDELL.NET

1-800-460-7733

PACKAGE LABEL DISPLAY:

ORAL SPRAYS

LIDDELL LABORATORIES
EST. 1994

Di
Diuretic

HOMEOPATHIC

1.0 FL. OZ. (30 ml)

Diuretic

DIURETIC
apis mellifica, berberis vulgaris, helleborus niger, juniperus communis, prunus spinosa, strophanthus hispidus, taraxacum officinale, uva-ursi spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50845-0106
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)	APIS MELLIFERA	3 [hp_X] in 1 mL
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	3 [hp_X] in 1 mL
HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815)	HELLEBORUS NIGER ROOT	3 [hp_X] in 1 mL
JUNIPERUS COMMUNIS WHOLE (UNII: 464910T5N9) (JUNIPERUS COMMUNIS WHOLE - UNII:464910T5N9)	JUNIPERUS COMMUNIS WHOLE	1 [hp_X] in 1 mL
PRUNUS SPINOSA FLOWER BUD (UNII: 53Y84VPS2W) (PRUNUS SPINOSA FLOWER BUD - UNII:53Y84VPS2W)	PRUNUS SPINOSA FLOWER BUD	3 [hp_X] in 1 mL
STROPHANTHUS HISPIDUS SEED (UNII: MO892VI77K) (STROPHANTHUS HISPIDUS SEED - UNII:MO892VI77K)	STROPHANTHUS HISPIDUS SEED	6 [hp_X] in 1 mL
TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375)	TARAXACUM OFFICINALE	1 [hp_X] in 1 mL
ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (ARCTOSTAPHYLOS UVA-URSI LEAF - UNII:3M5V3D1X36)	ARCTOSTAPHYLOS UVA-URSI LEAF	3 [hp_X] in 1 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50845-0106-1	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/02/2015	09/19/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		12/02/2015	09/19/2022

Labeler - Liddell Laboratories, Inc. (832264241)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(50845-0106) , api manufacture(50845-0106) , label(50845-0106) , pack(50845-0106)

Revised: 5/2022

Document Id: 81a62eef-9181-472f-b1b7-3bec6fdd4f3b

Set id: 2b6b72d0-8dfd-40b9-b789-b73b4100f1ad

Version: 5

Effective Time: 20220523

Liddell Laboratories, Inc.