LIVER DETOX

Manufacturer: Liddell Laboratories, Inc. | Apotheca Company
Effective date: 2024-07-01
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 02:27:28

Label at a glance#

ProductLIVER DETOX

Active ingredientBRYONIA ALBA ROOT, MILK THISTLE, CHELIDONIUM MAJUS WHOLE, PORK LIVER, TARAXACUM OFFICINALE

Label structure9 sections

Indications and uses

May temporarily relieve symptoms of a toxic liver, such as feelings of fatigue.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

Adults and children over 12 Spray twice under the tongue three times per day. Use daily for first month, then daily every other week. Children 12 and under Consult a doctor prior to use.

Contacts and useful links#

PhoneLabel contact1-800-460-7733

Websitewww.liddell.net

WWW.LIDDELL.NET

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

BRYONIA (ALBA) 200C, CARDUUS MARIANUS 1X, CHELIDONIUM MAJUS 200C, HEPAR SUIS 6X, TARAXACUM OFFICINALE 1X

USES:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of a toxic liver, such as feelings of fatigue.**

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

WARNINGS:

WARNINGS SECTION

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.

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

If pregnant or breast feeding, ask a doctor before using product.

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

Other information

Store at room temperature.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12

Spray twice under the tongue three times per day. Use daily for first month, then daily every other week.

Children 12 and under

Consult a doctor prior to use.

USES:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms of a toxic liver, such as feelings of fatigue.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 30% v/v, Purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY

LIDDELL LABORATORIES INC.

201 APPLE BLVD.

WOODBINE, IA 51579

www.LIDDELL.NET

1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL
LABORATORIES
EST. 1994

DETOX
57

LD
LIVER DETOX

May relieve symptoms
of a toxic liver
such as feelings of fatigue.

HOMEOPATHIC

DOCTOR FORMULATED
Readily absorbed. Safe.
No known side effects. Easy to use.

1.0 FL OZ. (30 ml)

Liver Detox lbl

Liver Detox ctn

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50845-0105-2	2024-07-01	C162847	48780-1	9d75b9d1-1f44-f424-e053-dadaa90a57ce	DRUG FACTS:
50845-0105-2	2024-01-30	C162847	48780-1	9d75b9d1-1f44-f424-e053-dadaa90a57ce	DRUG FACTS:
50845-0105-2	2021-12-20	C162847	48780-1	9d75b9d1-1f44-f424-e053-dadaa90a57ce	DRUG FACTS:
50845-0105-2	2020-01-31	C162847	48780-1	9d75b9d1-1f44-f424-e053-dadaa90a57ce	DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50845-0105-1	LIVER DETOX	30 mL in 1 BOTTLE, SPRAY	SPRAY	30		7
50845-0105-2	LIVER DETOX	1 in 1 CARTON	SPRAY	1		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50845-0105	LIVER DETOX (BRYONIA (ALBA), CARDUUS MARIANUS, CHELIDONIUM MAJUS, HEPAR SUIS, TARAXACUM OFFICINALE) SPRAY [LIDDELL LABORATORIES, INC.]	7	Current NDC, Legacy NDC, 2 package rows	20240702_e8337c7c-61fb-4c30-8814-13d90a6780b3.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
BRYONIA ALBA ROOT	ACTIVE INGREDIENT	T7J046YI2B	1
CHELIDONIUM MAJUS	ACTIVE INGREDIENT	7E889U5RNN	1
MILK THISTLE	ACTIVE INGREDIENT	U946SH95EE	1
PORK LIVER	ACTIVE INGREDIENT	6EC706HI7F	1
TARAXACUM OFFICINALE	ACTIVE INGREDIENT	39981FM375	1
BRYONIA ALBA ROOT	ACTIVE MOIETY	T7J046YI2B	1
CHELIDONIUM MAJUS	ACTIVE MOIETY	7E889U5RNN	1
MILK THISTLE	ACTIVE MOIETY	U946SH95EE	1
PORK LIVER	ACTIVE MOIETY	6EC706HI7F	1
TARAXACUM OFFICINALE	ACTIVE MOIETY	39981FM375	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

LIVER DETOX
Bryonia (Alba), Carduus Marianus, Chelidonium Majus, Hepar Suis, Taraxacum Officinale
BRYONIA ALBA ROOT
MILK THISTLE
CHELIDONIUM MAJUS WHOLE
CHELIDONIUM MAJUS
PORK LIVER
TARAXACUM OFFICINALE
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50845-0105	50845-0105-1, 50845-0105-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BRYONIA ALBA ROOT	T7J046YI2B	ACTIB
MILK THISTLE	U946SH95EE	ACTIB
CHELIDONIUM MAJUS WHOLE	7E889U5RNN	ACTIB
PORK LIVER	6EC706HI7F	ACTIB
TARAXACUM OFFICINALE	39981FM375	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 45 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / ORAL	198 mg		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SYRUP / ORAL		21000 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / ORAL		6624 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	ELIXIR / ORAL		13675 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / ORAL	150.68 mg/1ml		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	ELIXIR / ORAL		13675 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / ORAL	150.68 mg/1ml		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE, EXTENDED RELEASE / ORAL		8 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / SUBLINGUAL		397 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	ELIXIR / ORAL		13675 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SYRUP / ORAL		21000 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / SUBLINGUAL		397 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TOPICAL		3633 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TOPICAL		3633 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE, EXTENDED RELEASE / ORAL		8 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / ORAL	198 mg		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / NASAL		20 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / ORAL	210 mg/1ml		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / NASAL		20 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	TABLET, DELAYED RELEASE / ORAL	NA		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	TABLET, DELAYED RELEASE / ORAL	NA		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / ORAL		6624 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / ORAL	198 mg		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / ORAL	210 mg/1ml		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / NASAL		20 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / ORAL	150.68 mg/1ml		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	TABLET, DELAYED RELEASE / ORAL	NA		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE, EXTENDED RELEASE / ORAL		8 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / ORAL		6624 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SYRUP / ORAL		21000 mg	Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / SUBLINGUAL		397 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / ORAL	210 mg/1ml		Exact identifier — unii+route 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TOPICAL		3633 mg	Exact identifier — unii+dosage form 45 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii+route 45 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
LIVER DETOX	BRYONIA (ALBA), CARDUUS MARIANUS, CHELIDONIUM MAJUS, HEPAR SUIS, TARAXACUM OFFICINALE	Liddell Laboratories, Inc.	e8337c7c-61fb-4c30-8814-13d90a6780b3	2024-07-01	Warnings	Exact identifier ndc (package): 50845-0105-1 ndc (package): 50845-0105-2 ndc (product): 50845-0105 ndc11 (package): 50845010502 ndc11 (package): 50845010501 spl id: 8ccd02b7-365f-4a91-a957-407a5042dbe3 spl set id: e8337c7c-61fb-4c30-8814-13d90a6780b3

Reported adverse events (FAERS/openFDA)#

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