Home FDA labels 23bcbd5c-d5f0-4516-abdc-cecfb762ec6b Thymoplex 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 Thymoplex
Generic name COCHLEARIA ARMORACIA, ECHINACEA (ANGUSTIFOLIA), CONDURANGO, GINKGO BILOBA, PINUS SYLVESTRIS, PROPOLIS, SPLEEN (SUIS), TABEBUIA IMPETIGINOSA, THYMUS (BOVINE), BEE POLLEN, HEPAR SULPHURIS CALCAREUM, PHOSPHORICUM ACIDUM, LACHESIS MUTUS
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 1f4a9fda-c53e-4c0c-b624-aa48436c0aea
SPL ID 23bcbd5c-d5f0-4516-abdc-cecfb762ec6b
Version 3
Effective date 2024-10-18
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:22 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 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Thymoplex openfda.brand_name generic name COCHLEARIA ARMORACIA, ECHINACEA (ANGUSTIFOLIA), CONDURANGO, GINKGO BILOBA, PINUS SYLVESTRIS, PROPOLIS, SPLEEN (SUIS), TABEBUIA IMPETIGINOSA, THYMUS (BOVINE), BEE POLLEN, HEPAR SULPHURIS CALCAREUM, PHOSPHORICUM ACIDUM, LACHESIS MUTUS openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0564-1 openfda.package_ndc ndc product 43857-0564 openfda.product_ndc ndc11 package 43857056401 derived:openfda.package_ndc spl id 23bcbd5c-d5f0-4516-abdc-cecfb762ec6b id spl set id 1f4a9fda-c53e-4c0c-b624-aa48436c0aea set_id unii VP2CN2G7Y8 openfda.unii unii 8DS6G120HJ openfda.unii unii D65QWF3541 openfda.unii unii VB06AV5US8 openfda.unii unii 8XEJ88V2T8 openfda.unii unii Q1RGP4UB73 openfda.unii unii 92AMN5J79Y openfda.unii unii 6Y8XYV2NOF openfda.unii unii 3729L8MA2C openfda.unii unii VSW71SS07I openfda.unii unii 19FUJ2C58T openfda.unii unii E4GA8884NN openfda.unii unii 1MBW07J51Q 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 care 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 cool, dry place. WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by physician.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.