Home FDA labels b6b5ad58-404f-4376-a745-0fa897c5d064 Postpituapar openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Postpituapar
Generic name APIS MELLIFICA, ARSENICUM ALBUM, LACHESIS MUTUS, NUX VOMICA, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (PRATENSIS), SAMBUCUS NIGRA, THUJA OCCIDENTALIS
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 1212410f-ebe9-40b8-85f6-27bd45456e4a
SPL ID b6b5ad58-404f-4376-a745-0fa897c5d064
Version 6
Effective date 2024-10-29
Source export date 2026-10-12
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 03:13:00 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 17 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Postpituapar openfda.brand_name generic name APIS MELLIFICA, ARSENICUM ALBUM, LACHESIS MUTUS, NUX VOMICA, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (PRATENSIS), SAMBUCUS NIGRA, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0278-1 openfda.package_ndc ndc product 44911-0278 openfda.product_ndc ndc11 package 44911027801 derived:openfda.package_ndc spl id b6b5ad58-404f-4376-a745-0fa897c5d064 id spl set id 1212410f-ebe9-40b8-85f6-27bd45456e4a set_id unii 269XH13919 openfda.unii unii 7JM57I419K openfda.unii unii 1NT28V9397 openfda.unii unii S7V92P67HO openfda.unii unii 8E272251DI openfda.unii unii VSW71SS07I openfda.unii unii CT03BSA18U openfda.unii unii E4GA8884NN openfda.unii unii 7S82P3R43Z openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.