Spleenpar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:28:41

Label at a glance#

ProductSpleenpar
Active ingredientSUS SCROFA SPLEEN, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, CEANOTHUS AMERICANUS LEAF, QUININE SULFATE, STRYCHNOS IGNATII SEED, IODINE, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORIC ACID, PHOSPHORUS
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 9.09% of Arsenicum Album 12X, Carbo Vegetabilis 12X, Ceanothus Americanus 12X, Chininum Sulphuricum 12X, Ignatia Amara 12X, Iodium 12X, Natrum Muriaticum 12X, Nitricum Acidum 12X, Phosphoricum Acidum 12X, Phosphorus 12X, Spleen (Suis) 6X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve weakness, weariness, and flu-like symptoms.**

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

WARNINGS:

WARNINGS SECTION

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

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

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

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 contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional.

Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve weakness, weariness, and flu-like symptoms.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

SPLEENPAR

1 fl. oz. (30 ml)

SpleenparSpleenpar

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
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362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
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22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0261-12024-10-30C16284748780-1d6a99b39-a76c-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0261-12024-01-30C16284748780-1d6a99b39-a76c-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0261-12022-02-08C16284748780-1d6a99b39-a76c-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0261-12022-01-28C16284748780-1d6a99b39-a76c-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0261-1Spleenpar30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0261SPLEENPAR (SPLEEN (SUIS), ARSENICUM ALBUM, CARBO VEGETABILIS, CEANOTHUS AMERICANUS, CHININUM SULPHURICUM, IGNATIA AMARA, IODIUM, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUS) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20241101_f89581c5-faab-42b2-b984-e369f6ff8b49.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H101
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
CEANOTHUS AMERICANUS LEAFACTIVE INGREDIENT25B1Y14T8N1
IODINEACTIVE INGREDIENT9679TC07X41
NITRIC ACIDACTIVE INGREDIENT411VRN1TV41
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
QUININE SULFATEACTIVE INGREDIENTKF7Z0E0Q2B1
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487K1
SUS SCROFA SPLEENACTIVE INGREDIENT92AMN5J79Y1
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H101
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
CEANOTHUS AMERICANUS LEAFACTIVE MOIETY25B1Y14T8N1
CHLORIDE IONACTIVE MOIETYQ32ZN486981
IODINEACTIVE MOIETY9679TC07X41
NITRIC ACIDACTIVE MOIETY411VRN1TV41
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
PHOSPHORUSACTIVE MOIETY27YLU75U4W1
QUININEACTIVE MOIETYA7V27PHC7A1
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487K1
SUS SCROFA SPLEENACTIVE MOIETY92AMN5J79Y1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-026144911-0261-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 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
SpleenparSPLEEN (SUIS), ARSENICUM ALBUM, CARBO VEGETABILIS, CEANOTHUS AMERICANUS, CHININUM SULPHURICUM, IGNATIA AMARA, IODIUM, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUSEnergique, Inc.f89581c5-faab-42b2-b984-e369f6ff8b492024-10-30WarningsExact identifier
ndc (package): 44911-0261-1
ndc (product): 44911-0261
ndc11 (package): 44911026101
spl id: 9cdb1036-89a8-455a-ac56-be6742001ba4
spl set id: f89581c5-faab-42b2-b984-e369f6ff8b49

Reported adverse events (FAERS/openFDA)#

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