Degex Liquescence

Manufacturer
Nutritional Specialties, Inc.
Effective date
2025-05-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:33:33

Label at a glance#

ProductDegex Liquescence
Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG, UBIDECARENONE, CONIUM MACULATUM FLOWERING TOP, ASTERIAS RUBENS, GERMANIUM, LACHESIS MUTA VENOM, BUFO BUFO CUTANEOUS GLAND, HUMAN BREAST TUMOR CELL, PHOSPHORUS
Label structure9 sections

Dosage and administration

1/2 teaspoonful one to two times a day. Patients 12 years and under: Topical use only, to the navel area or forearm.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Thuja Occidentalis 6X, 9X, Ubidecarenonum (CoQ10) 8X, Conium Maculatum 9X, 12X, Asterias Rubens 12X, Germanium Metallicum 12X, Lachesis Mutus 12X, Bufo Rana 12X, 30X, Carcinosin 16X, 30X, Phosphorus 30X, 60X.

PURPOSE:

OTC - PURPOSE SECTION

Provides potentized homeo-nutritional support to aid in support of cellular function.†

†Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

Professional Use Only

If pregnant or breast-feeding, ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

If condition worsens, seek medical attention.

KEEP OUT OF REACH OF CHILDREN

Do not use if tamper evident seal is broken or missing.

Store in a cool place after opening

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1/2 teaspoonful one to two times a day. Patients 12 years and under: Topical use only, to the navel area or forearm.

INDICATIONS:

INDICATIONS & USAGE SECTION

Provides potentized homeo-nutritional support to aid in support of cellular function.†

†Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Alcohol USP 20%, Purified Water USP.

QUESTIONS:

OTC - QUESTIONS SECTION

MANUFACTURED EXCLUSIVELY FOR

NUTRITIONAL SPECIALTIES, INC.

PO BOX 97227

PITTSBURG, PA 15229

www.phpltd.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Professional

Health Products

HOMEOPATHIC

NDC 83027-0037-1

DEGEX

LIQUESCENCE

4 FL. OZ (120 ml)

DEGEX LIQUESCENCEDEGEX LIQUESCENCE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83027-0037-1Degex Liquescence120 mL in 1 BOTTLE, GLASSLIQUID1203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83027-0037DEGEX LIQUESCENCE (THUJA OCCIDENTALIS, UBIDECARENONUM, CONIUM MACULATUM, ASTERIAS RUBENS, GERMANIUM METALLICUM, LACHESIS MUTUS, BUFO RANA, CARCINOSIN, PHOSPHORUS) LIQUID [NUTRITIONAL SPECIALTIES, INC.]3Current NDC, 1 package rows20250516_c189b8ca-ef0a-41d5-98c1-eb0ecdba37c8.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83027-003783027-0037-1

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
Degex LiquescenceTHUJA OCCIDENTALIS, UBIDECARENONUM, CONIUM MACULATUM, ASTERIAS RUBENS, GERMANIUM METALLICUM, LACHESIS MUTUS, BUFO RANA, CARCINOSIN, PHOSPHORUSNutritional Specialties, Inc.c189b8ca-ef0a-41d5-98c1-eb0ecdba37c82025-05-15WarningsExact identifier
ndc (package): 83027-0037-1
ndc (product): 83027-0037
ndc11 (package): 83027003701
spl id: e4ae92ea-06a7-40e4-8566-7cd7e0c7ee84
spl set id: c189b8ca-ef0a-41d5-98c1-eb0ecdba37c8

Reported adverse events (FAERS/openFDA)#

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