Home FDA labels b55a39dd-d940-46ae-ab1f-8a9ef4a3413b Heart Small Intestine Meridian Opener 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 Heart Small Intestine Meridian Opener
Generic name ARSENICUM ALBUM, AURUM METALLICUM, CACTUS GRANDIFLORUS, CINCHONA OFFICINALIS, DIGITALIS PURPUREA, KALI CARBONICUM, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NAJA TRIPUDIANS, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), PYROGENIUM, SPIGELIA ANTHELMIA
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 0f398c70-455c-48be-9af3-3eccc96d99a1
SPL ID b55a39dd-d940-46ae-ab1f-8a9ef4a3413b
Version 1
Effective date 2025-05-06
Source export date 2026-10-12
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:32:29 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Heart Small Intestine Meridian Opener openfda.brand_name generic name ARSENICUM ALBUM, AURUM METALLICUM, CACTUS GRANDIFLORUS, CINCHONA OFFICINALIS, DIGITALIS PURPUREA, KALI CARBONICUM, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NAJA TRIPUDIANS, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), PYROGENIUM, SPIGELIA ANTHELMIA openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2265-1 openfda.package_ndc ndc product 43742-2265 openfda.product_ndc ndc11 package 43742226501 derived:openfda.package_ndc spl id b55a39dd-d940-46ae-ab1f-8a9ef4a3413b id spl set id 0f398c70-455c-48be-9af3-3eccc96d99a1 set_id unii 27YLU75U4W openfda.unii unii 269XH13919 openfda.unii unii 324Y4038G2 openfda.unii unii 29SUH5R3HU openfda.unii unii 79Y1949PYO openfda.unii unii BQN1B9B9HA openfda.unii unii S7V92P67HO openfda.unii unii WYT05213GE openfda.unii unii 8E272251DI openfda.unii unii S003A158SB openfda.unii unii ZZ4AG7L7VM openfda.unii unii F1T8QT9U8B openfda.unii unii 2BMD2GNA4V openfda.unii unii C88X29Y479 openfda.unii unii 7114SV0MYK 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 breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.