Cholenest

Manufacturer
Marco Pharma International LLC. | Nestmann Pharma GmbH
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:36:43

Label at a glance#

ProductCholenest
Active ingredientFRANGULA PURSHIANA BARK, SILYBUM MARIANUM SEED, TARAXACUM OFFICINALE, CHELIDONIUM MAJUS, VERONICASTRUM VIRGINICUM ROOT, MORELLA CERIFERA ROOT BARK, BERBERIS VULGARIS ROOT BARK, SODIUM SULFATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, COPPER
Label structure2 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Cascara sagrada 1xHPUS

Milk thistle 1xHPUS

Dandelion 1xHPUS

Celadine 1xHPUS

Culver's root 2xHPUS

Bayberry 2xHPUS

Barberry 2xHPUS

Disodium sulfate 6xHPUS

Magnesium hydrogen phosphate 8xHPUS

Metallic copper 8XHPUS

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

Purpose

OTC - PURPOSE SECTION

Relief of constipation, difficulty digesting fat.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Suggested use

INDICATIONS & USAGE SECTION

Adults: 30-40 drops in tepid water 3 times daily before meals. Children, 10 drops in tepid water 3 times daily before meals.

Warnings

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

(Read Suggested Use Section)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ethyl Alcohol (63.3% by vol.) and Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

N14_60986-1008-3-4N14_60986-1008-3-4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
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726062af-1135-4707-a1d7-57256991bbf9Product name220250226
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efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
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9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
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6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
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8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
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c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60986-1008-32020-12-04C16284748780-19d75b9d0-edee-f424-e053-dadaa90a57ceDrug Facts
60986-1008-42020-12-04C16284748780-19d75b9d0-edee-f424-e053-dadaa90a57ceDrug Facts
60986-1008-32020-01-31C16284748780-19d75b9d0-edee-f424-e053-dadaa90a57ceDrug Facts
60986-1008-42020-01-31C16284748780-19d75b9d0-edee-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60986-1008-3Cholenest50 mL in 1 BOTTLE, GLASSLIQUID507
60986-1008-4Cholenest100 mL in 1 BOTTLE, GLASSLIQUID1007

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BERBERIS VULGARIS ROOT BARKACTIVE INGREDIENT1TH8Q20J0U1
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNN1
COPPERACTIVE INGREDIENT789U1901C51
FRANGULA PURSHIANA BARKACTIVE INGREDIENT4VBP01X99F1
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATEACTIVE INGREDIENTHF539G9L3Q1
MORELLA CERIFERA ROOT BARKACTIVE INGREDIENTS46HJ3710D1
SILYBUM MARIANUM SEEDACTIVE INGREDIENTU946SH95EE1
SODIUM SULFATEACTIVE INGREDIENT0YPR65R21J1
TARAXACUM OFFICINALEACTIVE INGREDIENT39981FM3751
VERONICASTRUM VIRGINICUM ROOTACTIVE INGREDIENTM2O62YTN421
BERBERIS VULGARIS ROOT BARKACTIVE MOIETY1TH8Q20J0U1
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNN1
COPPERACTIVE MOIETY789U1901C51
FRANGULA PURSHIANA BARKACTIVE MOIETY4VBP01X99F1
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY8381
MORELLA CERIFERA ROOT BARKACTIVE MOIETYS46HJ3710D1
SILYBUM MARIANUM SEEDACTIVE MOIETYU946SH95EE1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
TARAXACUM OFFICINALEACTIVE MOIETY39981FM3751
VERONICASTRUM VIRGINICUM ROOTACTIVE MOIETYM2O62YTN421
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60986-100860986-1008-3, 60986-1008-4

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
CholenestRHAMNUS PURSHIANA, CARDUUS MARIANUS, TARAXACUM OFFICINALE, CHELIDONIUM MAJUS, LEPTANDRA VIRGINICA, MYRICA CERIFERA, BERBERIS VULGARIS, NATRUM SULPHURICUM, MAGNESIA PHOSPHORICA, CUPRUM METALLICUMMarco Pharma International LLC.4b89ffcb-318b-416d-b13c-19fb94c2af702026-01-12WarningsExact identifier
ndc (package): 60986-1008-4
ndc (package): 60986-1008-3
ndc (product): 60986-1008
ndc11 (package): 60986100803
ndc11 (package): 60986100804
spl id: 483c66da-6d99-08e2-e063-6294a90aeb8b
spl set id: 4b89ffcb-318b-416d-b13c-19fb94c2af70

Reported adverse events (FAERS/openFDA)#

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