Home FDA labels a0227bfa-5617-4620-8a57-4ffb3a724033 Resentment 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 Resentment
Generic name ADRENALINUM, AMMONIUM MURIATICUM, APOCYNUM CANNABINUM, BUTHUS AUSTRALIS, CARDUUS MARIANUS, CINCHONA OFFICINALIS, FEL TAURI, HEPAR SUIS, HEPAR SULPHURIS CALCAREUM, HYPOTHALAMUS SUIS, MANGANUM CARBONICUM, MOSCHUS, NAJA TRIPUDIANS, NATRUM MURIATICUM, NITRICUM ACIDUM, NUX VOMICA, RHUS TOX, TARAXACUM OFFICINALE
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID d397ed9c-10f0-4a99-baca-a31e5e18572a
SPL ID a0227bfa-5617-4620-8a57-4ffb3a724033
Version 2
Effective date 2025-05-27
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:28:58 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Resentment openfda.brand_name generic name ADRENALINUM, AMMONIUM MURIATICUM, APOCYNUM CANNABINUM, BUTHUS AUSTRALIS, CARDUUS MARIANUS, CINCHONA OFFICINALIS, FEL TAURI, HEPAR SUIS, HEPAR SULPHURIS CALCAREUM, HYPOTHALAMUS SUIS, MANGANUM CARBONICUM, MOSCHUS, NAJA TRIPUDIANS, NATRUM MURIATICUM, NITRICUM ACIDUM, NUX VOMICA, RHUS TOX, TARAXACUM OFFICINALE openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2244-1 openfda.package_ndc ndc product 43742-2244 openfda.product_ndc ndc11 package 43742224401 derived:openfda.package_ndc spl id a0227bfa-5617-4620-8a57-4ffb3a724033 id spl set id d397ed9c-10f0-4a99-baca-a31e5e18572a set_id unii 01Q9PC255D openfda.unii unii 269XH13919 openfda.unii unii ET3651ZLOU openfda.unii unii 411VRN1TV4 openfda.unii unii 8KFK4W7KP7 openfda.unii unii 39981FM375 openfda.unii unii U946SH95EE openfda.unii unii 451W47IQ8X openfda.unii unii YKH834O4BH openfda.unii unii 6IO182RP7A openfda.unii unii S003A158SB openfda.unii unii 25IMQ489AW openfda.unii unii ZZ4AG7L7VM openfda.unii unii 9ZV57512ZM openfda.unii unii 2F92409L9Z openfda.unii unii 6EC706HI7F openfda.unii unii 1MBW07J51Q 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.