Home FDA labels 4ce0643f-2459-4c94-bfbe-6d4d12f89339 Resilience 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 Resilience
Generic name CEREBRUM SUIS, HYPOTHALAMUS SUIS, HYPOPHYSIS SUIS, SEROTONIN (HYDROCHLORIDE), NPY (NEUROPEPTIDE Y), CALCAREA CARBONICA, SILICEA, VERATRUM ALBUM, BLATTA AMERICANA, CACAO, DIOSPYROS KAKI, FORMICA RUFA, PALOONDO, SULPHUR, TAXUS BACCATA, TELA ARANEAE, SALIX VITELLINA, FLOS
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 3aa6c1e7-2bd9-4c2d-bfd4-63ffb7c62e9c
SPL ID 4ce0643f-2459-4c94-bfbe-6d4d12f89339
Version 1
Effective date 2026-02-26
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 05:48:45 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Resilience openfda.brand_name generic name CEREBRUM SUIS, HYPOTHALAMUS SUIS, HYPOPHYSIS SUIS, SEROTONIN (HYDROCHLORIDE), NPY (NEUROPEPTIDE Y), CALCAREA CARBONICA, SILICEA, VERATRUM ALBUM, BLATTA AMERICANA, CACAO, DIOSPYROS KAKI, FORMICA RUFA, PALOONDO, SULPHUR, TAXUS BACCATA, TELA ARANEAE, SALIX VITELLINA, FLOS openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2295-1 openfda.package_ndc ndc product 43742-2295 openfda.product_ndc ndc11 package 43742229501 derived:openfda.package_ndc spl id 4ce0643f-2459-4c94-bfbe-6d4d12f89339 id spl set id 3aa6c1e7-2bd9-4c2d-bfd4-63ffb7c62e9c set_id unii XBP5X7E70R openfda.unii unii 6LK42KUV6W openfda.unii unii 4GB5DQR532 openfda.unii unii GKN429M9VS openfda.unii unii BY7U39XXK0 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii L0PFEMQ1DT openfda.unii unii 55H0W83JO5 openfda.unii unii 2E32821G6I openfda.unii unii D9108TZ9KG openfda.unii unii 2RQ1L9N089 openfda.unii unii 70FD1KFU70 openfda.unii unii 4V023DD7KL openfda.unii unii QNS6W5US1Z openfda.unii unii 98689CD777 openfda.unii unii PK0TXD049P openfda.unii unii N6R0856Z79 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.