Postpituapar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:28:33

Label at a glance#

ProductPostpituapar
Active ingredientAPIS MELLIFERA, ARSENIC TRIOXIDE, LACHESIS MUTA VENOM, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, BOS TAURUS PITUITARY GLAND, POSTERIOR, PULSATILLA PRATENSIS WHOLE, SAMBUCUS NIGRA FLOWERING TOP, THUJA OCCIDENTALIS LEAFY TWIG
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): 11.11% of Apis Mellifica 12X, Arsenicum Album 12X, Lachesis Mutus 12X, Nux Vomica 12X, Phosphoricum Acidum 12X, Pituitarum Posterium (Bovine) 12X, Pulsatilla (Pratensis) 12X, Sambucus Nigra 12X, Thuja Occidentalis 12X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve weakness, lethargy and frequent urination.**

**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, lethargy and frequent urination.**

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

POSTPITUAPAR

1 fl. oz. (30 ml)

POSTPITUAPARPOSTPITUAPAR

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0278-12024-10-29C16284748780-1ba0f9c33-2998-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0278-12024-01-30C16284748780-1ba0f9c33-2998-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0278-12022-03-02C16284748780-1ba0f9c33-2998-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0278-12021-01-29C16284748780-1ba0f9c33-2998-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0278-1Postpituapar30 mL in 1 BOTTLE, DROPPERLIQUID306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0278POSTPITUAPAR (APIS MELLIFICA, ARSENICUM ALBUM, LACHESIS MUTUS, NUX VOMICA, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (PRATENSIS), SAMBUCUS NIGRA, THUJA OCCIDENTALIS) LIQUID [ENERGIQUE, INC.]6Current NDC, Legacy NDC, 1 package rows20241031_1212410f-ebe9-40b8-85f6-27bd45456e4a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
PULSATILLA PRATENSISACTIVE INGREDIENT8E272251DI1
SAMBUCUS NIGRA FLOWERING TOPACTIVE INGREDIENTCT03BSA18U1
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
SUS SCROFA PITUITARY GLANDACTIVE INGREDIENTE8S87O660T1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
PULSATILLA PRATENSISACTIVE MOIETY8E272251DI1
SAMBUCUS NIGRA FLOWERING TOPACTIVE MOIETYCT03BSA18U1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
SUS SCROFA PITUITARY GLANDACTIVE MOIETYE8S87O660T1
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 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-027844911-0278-1

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

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
PostpituaparAPIS MELLIFICA, ARSENICUM ALBUM, LACHESIS MUTUS, NUX VOMICA, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (PRATENSIS), SAMBUCUS NIGRA, THUJA OCCIDENTALISEnergique, Inc.1212410f-ebe9-40b8-85f6-27bd45456e4a2024-10-29WarningsExact identifier
ndc (package): 44911-0278-1
ndc (product): 44911-0278
ndc11 (package): 44911027801
spl id: b6b5ad58-404f-4376-a745-0fa897c5d064
spl set id: 1212410f-ebe9-40b8-85f6-27bd45456e4a

Reported adverse events (FAERS/openFDA)#

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