Lymphonest

Manufacturer
Marco Pharma International LLC. | Marco Pharma International LLC | Nestmann Pharma GmbH
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:36:44

Label at a glance#

ProductLymphonest
Active ingredientECHINACEA ANGUSTIFOLIA, SCROPHULARIA NODOSA, ARTEMISIA ABROTANUM FLOWERING TOP, KEROSENE, ALOE, MERCURIUS SOLUBILIS, CROTALUS HORRIDUS HORRIDUS VENOM, THUJA OCCIDENTALIS LEAFY TWIG, LACHESIS MUTA VENOM, ARISTOLOCHIA CLEMATITIS ROOT
Label structure2 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Coneflower 1x HPUS

Figwort 1x HPUS

Southernwood 3x HPUS

Kerosine 3x HPUS

Cape Aloe 1x HPUS

Hahnemann's soluble mercury 12x HPUS

Timber rattlesnake 10x HPUS

White cedar 10x HPUS

Bushmaster Viper 8x HPUS

Birthwort 6x HPUS

The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.

Purpose

OTC - PURPOSE SECTION

For relief of swollen lymph glands; suppressed immune functions.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Suggested use

INDICATIONS & USAGE SECTION

30 drops in water 3 times daily. In acute stages, take 50 drops at once followed by 30 drops 4 times daily. Children receive one half or less of the adult amount.

Warnings

WARNINGS SECTION

If pregnant or breast-feeding, consult a health professional before use. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

DOSAGE & ADMINISTRATION SECTION

(Read Suggested Use Section)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ethyl Alcohol (63% by vol.) and Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

N10_60986-1004-3-4N10_60986-1004-3-4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60986-1004-32020-12-03C16284748780-19d75b9d0-e1eb-f424-e053-dadaa90a57ceDrug Facts
60986-1004-42020-12-03C16284748780-19d75b9d0-e1eb-f424-e053-dadaa90a57ceDrug Facts
60986-1004-32020-01-31C16284748780-19d75b9d0-e1eb-f424-e053-dadaa90a57ceDrug Facts
60986-1004-42020-01-31C16284748780-19d75b9d0-e1eb-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60986-1004-3Lymphonest50 mL in 1 BOTTLE, GLASSLIQUID506
60986-1004-4Lymphonest100 mL in 1 PACKAGELIQUID1006

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALOEACTIVE INGREDIENTV5VD430YW91
ARISTOLOCHIA CLEMATITIS ROOTACTIVE INGREDIENTZY0NX0W00D1
ARTEMISIA ABROTANUM FLOWERING TOPACTIVE INGREDIENTQG07G580U01
CROTALUS HORRIDUS HORRIDUS VENOMACTIVE INGREDIENTYHA2XLJ9561
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US81
KEROSENEACTIVE INGREDIENT1C89KKC04E1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
MERCURIUS SOLUBILISACTIVE INGREDIENT324Y4038G21
SCROPHULARIA NODOSAACTIVE INGREDIENT7H443NUB2T1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
ALOEACTIVE MOIETYV5VD430YW91
ARISTOLOCHIA CLEMATITIS ROOTACTIVE MOIETYZY0NX0W00D1
ARTEMISIA ABROTANUM FLOWERING TOPACTIVE MOIETYQG07G580U01
CROTALUS HORRIDUS HORRIDUS VENOMACTIVE MOIETYYHA2XLJ9561
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US81
KEROSENEACTIVE MOIETY1C89KKC04E1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
MERCURIUS SOLUBILISACTIVE MOIETY324Y4038G21
SCROPHULARIA NODOSAACTIVE MOIETY7H443NUB2T1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V93971
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60986-100460986-1004-3, 60986-1004-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

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 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
3 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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LymphonestECHINACEA AUGUSTIFOLIA, SCROPHULARIA NODOSA, ABROTANUM, PETROLEUM, ALOE SOCOTRINA, MERCURIUS SOLUBILIS, CROTALUS HORIIDUS, THUJA OCCIDENTALIS, LACHESIS MUTUS, ARISTOLOCHIA CLEMATITISMarco Pharma International LLC.84e18e97-4892-4699-b0c6-c194dc783b2d2026-01-12WarningsExact identifier
ndc (package): 60986-1004-4
ndc (package): 60986-1004-3
ndc (product): 60986-1004
ndc11 (package): 60986100403
ndc11 (package): 60986100404
spl id: 483c2be0-953e-7ce6-e063-6394a90a3fcd
spl set id: 84e18e97-4892-4699-b0c6-c194dc783b2d

Reported adverse events (FAERS/openFDA)#

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