Home FDA labels e61360cc-da3b-4d07-962f-3d6d903d892a Grief 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 Grief
Generic name CIMICIFUGA RACEMOSA, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM, SEPIA, CEREBRUM SUIS, IGNATIA AMARA, NATRUM MURIATICUM, AMBRA GRISEA, DNA, AURUM METALLICUM, COCCULUS INDICUS, DIGITALIS PURPUREA, HELLEBORUS NIGER, LYCOPODIUM CLAVATUM, STAPHYSAGRIA
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID e7ff1297-512e-4e95-a918-1c57fa3a50dd
SPL ID e61360cc-da3b-4d07-962f-3d6d903d892a
Version 4
Effective date 2024-03-25
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:48:46 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 Grief openfda.brand_name generic name CIMICIFUGA RACEMOSA, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM, SEPIA, CEREBRUM SUIS, IGNATIA AMARA, NATRUM MURIATICUM, AMBRA GRISEA, DNA, AURUM METALLICUM, COCCULUS INDICUS, DIGITALIS PURPUREA, HELLEBORUS NIGER, LYCOPODIUM CLAVATUM, STAPHYSAGRIA openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1513-1 openfda.package_ndc ndc product 43742-1513 openfda.product_ndc ndc11 package 43742151301 derived:openfda.package_ndc spl id e61360cc-da3b-4d07-962f-3d6d903d892a id spl set id e7ff1297-512e-4e95-a918-1c57fa3a50dd set_id unii 4GB5DQR532 openfda.unii unii 51FI676N6F openfda.unii unii 00543AP1JV openfda.unii unii 0YPR65R21J openfda.unii unii QDL83WN8C2 openfda.unii unii 608DGJ6815 openfda.unii unii 451W47IQ8X openfda.unii unii 1NM3M2487K openfda.unii unii 79Y1949PYO openfda.unii unii XTC0D02P6C openfda.unii unii 810258W28U openfda.unii unii E4GA8884NN openfda.unii unii F1T8QT9U8B openfda.unii unii C88X29Y479 openfda.unii unii K73E24S6X9 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, 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.