Home FDA labels 0ee2115f-c0ba-44fe-a39c-dc5a28cb301a ENT Support 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 ENT Support
Generic name ARGENTUM NITRICUM, ASPERGILLUS NIGER, CANDIDA ALBICANS, EUPHORBIUM OFFICINARUM, GALLICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, INFLUENZINUM (2024 - 2025), LUFFA OPERCULATA, MERCURIUS IODATUS RUBER, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH), PULSATILLA (PRATENSIS), SINUSITISINUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID fd8675cb-33c7-49bb-a035-f7c7881115f2
SPL ID 0ee2115f-c0ba-44fe-a39c-dc5a28cb301a
Version 1
Effective date 2026-02-23
Source export date 2026-11-06
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 07:17:40 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name ENT Support openfda.brand_name generic name ARGENTUM NITRICUM, ASPERGILLUS NIGER, CANDIDA ALBICANS, EUPHORBIUM OFFICINARUM, GALLICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, INFLUENZINUM (2024 - 2025), LUFFA OPERCULATA, MERCURIUS IODATUS RUBER, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH), PULSATILLA (PRATENSIS), SINUSITISINUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2358-1 openfda.package_ndc ndc product 43742-2358 openfda.product_ndc ndc11 package 43742235801 derived:openfda.package_ndc spl id 0ee2115f-c0ba-44fe-a39c-dc5a28cb301a id spl set id fd8675cb-33c7-49bb-a035-f7c7881115f2 set_id unii PS2DCE2WVF openfda.unii unii 48339473OT openfda.unii unii 1TI1O9028K openfda.unii unii 95IT3W8JZE openfda.unii unii 4D7G21HDBC openfda.unii unii AU5C98U4BB openfda.unii unii 17RH99LQ7G openfda.unii unii B575563DM5 openfda.unii unii C4MO6809HU openfda.unii unii CYK5P89K8X openfda.unii unii 8E272251DI openfda.unii unii 9IOA40ANG6 openfda.unii unii 514B9K0L10 openfda.unii unii R03O05RB0P openfda.unii unii 6TU4EY6UNW 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 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. 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 a physician. 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.